372 Medical Affairs Jobs

You will be working as a full-time Medical Records Executive at Ahalia Hospitals in Palghat, Kerala. Your primary responsibility will be to manage and maintain patient records, ensuring accurate and secure storage of medical information. This includes organizing and updating patient files, processing requests for medical records, and ensuring compliance with healthcare regulations and privacy laws. Close collaboration with healthcare professionals is essential to support efficient healthcare delivery and patient care. To excel in this role, you should possess skills in Medical Affairs and Medicine, along with experience in Healthcare Management and Strategic Planning. Proficiency in conducting and utilizing research, excellent organizational and detail-oriented skills, and familiarity with healthcare regulations and patient privacy laws are crucial. Strong interpersonal and communication skills are required for effective teamwork and collaboration. Any relevant certification or experience in medical records management would be advantageous. The ideal candidate for this position should have an M.Sc. in Medical Documentation. The job location is Palakkad, Kerala, and immediate joiners are preferred.,

Collaboration with Key Opinion Leaders (KOLs): Build and maintain relationships with Leading Specialists to understand customer needs and tailor medical activities accordingly. Engage in round tables , advisory boards , and medical education programs (approximately 20% of your time will be dedicated to direct interactions with KOLs). Medical Affairs Strategy: Contribute to the Medical Affairs Plan , including budget monitoring, by providing strategic input on medical programs, product positioning, and market insights. Be an active member of the cross-functional value team (CVT) and local action team (LAT) . Pre-launch and Post-launch Activities: Develop and implement pre-launch medical strategies and lead the design and facilitation of educational programs and presentations for both internal teams and external stakeholders, focusing on clinical data and the value propositions of new products. Compliance Regulatory Standards: Ensure all activities are in full compliance with Johnson Johnson s Credo and Health Care Business Integrity (HCBI) principles to preserve trust and reputation in the market. Medical Content Development: Contribute to the development and review of promotional and educational materials for internal and external use, ensuring scientific accuracy and compliance with relevant regulatory standards. Qualifications: Required: Medical Doctor (MD) , PhD , or a Pharmaceutical/Natural Science degree (with an MD/PhD being an additional asset). 2-4 years of relevant experience in medical affairs, clinical gastroenterology, or a related field. Deep understanding of clinical gastroenterology , including scientific research, clinical trial design, data interpretation, and strategy formulation. Proficiency in English and at least one of the following languages: German or French . Strong critical and strategic thinking skills, with the ability to translate scientific advancements into actionable medical affairs strategies and tactics. Excellent communication skills and the ability to engage with HCPs on a peer-to-peer level. Preferred: Experience in designing and leading medical programs , working with cross-functional teams , and executing medical education initiatives. A collaborative mindset, with the ability to build professional working relationships across various departments and geographies.

As the companys subject matter expert on drug safety and pharmacovigilance, you will be responsible for ensuring compliance with Local & Global PV-relevant Heath Authority requirements. Your role will involve overseeing PV Contracts, vendor management, and PV system audits/inspections. Additionally, you will develop a good understanding of signal management and benefit-risk evaluation activities. You will be expected to develop and implement Risk Management Plans (RMPs) and additional Risk mitigation measures. Acting as the primary safety liaison with country regulatory authorities and internal stakeholders will be a key part of your responsibilities. Collaboration with Clinical Development, Regulatory Affairs, Medical Affairs, Quality Assurance, marketing teams, etc., will also be essential. Your contribution to clinical trial safety strategies and protocols, including protocols, safety monitoring plans, and SAE reporting, will be crucial. Moreover, mentoring and developing PV team members to maintain a culture of continuous improvement and compliance will be part of your role. You will also manage departmental budgets, staffing, and resourcing in line with organizational needs. Qualifications: - Advanced degree in Medicine or Pharmacy - Minimum 10 years of progressive pharmacovigilance experience in the pharmaceutical industry - In-depth understanding of Local/global PV regulations and guidance - Demonstrated experience in leadership roles with proven ability to build and scale PV systems - Strong analytical, strategic thinking, and communication skills.,

As the Associate Director, Global Channel Analytics at GSK, you will be responsible for tracking, analyzing, and reporting on channel and content performance metrics within the Global Scientific Communications organization. Your role will involve providing actionable insights to optimize scientific communication strategies across therapeutic areas. Collaboration with Digital and Medical teams will be key to integrating generative AI tools into omnichannel content workflows, enhancing engagement, efficiency, and personalization. Your key responsibilities will include tracking, analyzing, and reporting on metrics and analytics across key scientific communication channels to improve channel and content engagement. You will synthesize complex analytics into data storytelling, shaping content planning and dissemination strategies through clear data-backed recommendations. Developing and maintaining metrics-driven narratives for reporting on integrated medical communication plans will involve collaborating with Digital teams for robust data visualization. Collaboration across the Scientific Communications team and Digital team will be essential to assess channel performance across various platforms, ensuring alignment with evolving content dissemination approaches. You will also identify performance trends and share strategic recommendations to optimize channel selection, audience targeting, and engagement approaches for scientific communications deliverables. Leveraging generative AI tools to enhance analytic efficiency will be a core aspect of your role, including monitoring AI-generated content performance and refining AI model tools in collaboration with Digital based on audience engagement metrics. To be successful in this role, you should have an advanced degree in science, medicine, pharmacy, or a related field, along with 5-7 years of related experience in scientific communications, analytics, and/or medical affairs. Proficiency in data visualization tools and experience leveraging insights to drive scientific communications strategies is required. Strong understanding of generative AI, cross-functional collaboration skills, problem-solving abilities, and technical capabilities in Excel, PowerPoint, and Team sites are essential. Preferred qualifications include a postgraduate degree, local, regional, or global medical or R&D experience with expertise in therapeutic areas, and experience with scientific communication strategies in large global markets. GSK is committed to inclusion, and adjustments can be made during the recruitment process by reaching out to the Recruitment Team. GSK is dedicated to uniting science, technology, and talent to positively impact the health of billions of people and deliver sustainable returns. Join GSK in its mission to prevent and treat diseases and create a thriving environment where people can excel and grow.,

To provide functional and operational directions to internalize HEOR analysis and comparative effectiveness analysis (meta-analysis, network-meta-analysis, indirect treatment comparison, matching adjusted indirect treatment comparison etc) processes in partnership with Global HEVA / ITC-NMA / Evidence Synthesis / Market Access / Medical teams. People: (1) Support Manager/Team Lead in collaboration with Global HEVA / ITC-NMA / Evidence Synthesis / Market Access / Medical teams to formulate and conduct analysis as per the requirement; (2) Maintain effective partnership with end stakeholders for the allocated GBU and products - with an end objective to develop appropriate comparative efficacy evidences to be used for internal decision making and for external audiences at product launch and over product life cycle; (3) Consistently assist team members in developing new knowledge and sharing expertise. Performance: (1) Provide inputs to the strategic development and execution of industry leading comparative efficacy analysis /HEOR study plan; (2) Work on methodological aspect of comparative effectiveness analysis (3) Provide strategic inputs in HEOR analysis activities; (4) Lead and support development of tools, technology, and processes in order to constantly improve quality and productivity; (5) Develop and maintain expertise across therapeutic areas/franchises. Process: (1) Assist in development of processes and templates to meet requirements and deliverables for HEVA comparative efficacy analysis across portfolio; (2) Support delivery of projects in terms of resourcing, quality, timeliness, efficiency, and high technical standards; (3) Secure adherence to comparative efficacy analysis guidelines and protocols; (4) Ensure creating and developing tools, technology, and process to constantly improve quality and productivity Stakeholder: (1) Maintain effective relationship with the end stakeholders (medical scientific community) with an end objective to develop education and communication content as per requirement; and (2) Partner with HEVA, Real World Evidence, Clinical, Medical Affairs, Marketing, External Affairs, and Market Access global or local teams, and interact effectively with external advisors About you Experience : 5+ years of experience in doing HEOR analytics which includes conducting comparative effectiveness analysis (NMA, ITC, MAIC etc) for HTA submissions, conducting feasibility analysis, and developing statistical analysis plan. Soft skills : Stakeholder management; communication skills; people management; and ability to influence and negotiate Technical skills : Advanced level training/experience in conducting comparative efficacy analysis (meta-analysis, NMA, ITC, MAIC etc)., hands-on experience of working with Excel VBA, familiarity with R, R-shiny, WinBugs. Education : Advanced degree in life sciences/ pharmacy/ health economics/ statistics/ Engineering or medical degree or related discipline Languages : Excellent knowledge of English language (spoken and written)

The Pharmacovigilance (PV) Science Expert is a global role, and it supports an international, dynamic, and culturally diverse team dedicated to safety surveillance throughout the product lifecycle of a broad range of products. The PV Science Expert is a safety expert who is responsible for performing core pharmacovigilance activities on a product, in partnership with the Global Safety Lead/Managers (GSLs/GSMs), to identify safety signals, evaluate, and analyze safety data for both marketed products and products in post marketing and clinical development. Accountabilities: -Manages ongoing core signal detection activities for Global Safety Leads/Managers (GSLs/GSMs) review (involve synthesis of data from multiple sources: PV database, literature, PV textbooks and external DBs) -Coordinates and authors draft health hazard evaluations (HHEs) and/or safety evaluation reports (SERs) -Primarily manages entry and tracking of signals, ME, INR in SMART tool and support GSLs/GSMs with any SMART related activities. -Reviews periodic signal detection reports (NINR, UDR, SD reports for PBRERs) -Contributes to responses to Health Authority questions or inquiries from internal or external stakeholders in collaboration with the Safety Team; includes proposing a strategy for the response review of relevant data. -Is a Core member of the Safety Management Committee (SMC) who contributes to produce the necessary data outputs, prepares slide presentations. -Supports GSL/GSM to provide safety content for new drug applications and other regulatory filings including review of the safety and benefit risk sections to ensure consistency across documents and support response preparation -Supports GSL/GSM in drafting of the safety sections of the EU Risk Management Plan (RMPs) for Safety Team for review and comment. -Contributes to risk assessment and benefit risk assessment for marketed products (Scheduling and coordinating meetings/ Drafting meeting agenda and minutes/Tracking action items and soliciting follow-up for open issues). -Collaboration with various stakeholders including but not limited to PV Quality, Medical Safety, QPPV and PV Operations, Medical affairs, Labeling, Regulatory affairs and PV vendors. -Provide OTC SWITCH SER Support. -Supports in mentoring of new PV safety scientists (PVSs). -Supports in audit and inspection preparation. -Helping in management of process related queries at user level. -Acting in the capacity of lead, which may entail serving as the primary point of contact, negotiating deliverable timelines, and resolving project related issues. Experience : Working knowledge of drug safety and risk management including 5-8 years industry experience, and understanding of drug development, basic knowledge of regulatory guidelines and medical coding. Soft skills : Stakeholder management, Strong negotiation and communication skills, and ability to operate effectively in a global environment and across-line functions. Excellent organizational and project management abilities. Strong communication and interpersonal skills. Ability to work effectively in a cross-functional, multicultural environment. Think strategically and lead teams Technical skills : Evaluation, interpretation, and synthetization of scientific data Knowledge of pharmacovigilance practices including US and EU pharmacovigilance regulatory requirements appreciated Signal Risk Management: Expertise in the collection of drug safety information from a variety of sources throughout the product life cycle to proactively detect, validate, and assess potential signals appreciated Proficient in international regulations, guidelines good practices pertaining to the pharmaceutical industry standard and practices in pharmacovigilance Works well in a team setting as well as independently. High attention to detail with exceptional writing, logical and problem-solving abilities. Eagerness to learn. Excellent individual veracity, with a solid personal commitment to follow all guidelines, protocols, Standard Operating Procedures and the companys values and ethics, as well as comply with pharma Codes and regulations. Ability to collaborate between different teams and functions. Excellent networking and influencing skills Education : Preferred health care discipline degree in modern science: Masters in Pharmacy, Master of Health Science, Physician Assistant, MBBS, BDS etc Languages : Fluent in English (verbal and written)

As a Patient Relations Specialist in Oncology at Vaidam Health, you will play a crucial role in assisting patients and healthcare providers by coordinating appointments, maintaining patient records, and ensuring effective communication throughout the treatment process. Located in Gurugram, this full-time on-site position requires a dedicated individual with a background in Medical Affairs and Medicine, specifically in Oncology. Your responsibilities will include managing patient inquiries, organizing medical travel arrangements, and collaborating with doctors to facilitate pre-treatment consultations and post-treatment follow-ups. Your expertise in patient care coordination, combined with excellent communication and interpersonal skills, will contribute to maintaining a high level of patient satisfaction and care quality. To excel in this role, you should possess a Bachelor's degree in a healthcare-related field or demonstrate relevant experience in the medical domain. Strong research skills, the ability to work independently and juggle multiple tasks, as well as proficiency in using healthcare management software and tools, are essential qualifications for this position. Join our dynamic team at Vaidam Health and be part of a global network that has assisted over 100,000 patients from 125+ countries. Make a difference in the lives of medical travelers worldwide by providing essential support and guidance throughout their treatment journey.,

We are looking for the Primary scientific face of the organization to Thought Leaders & physicians for a given therapy area. You will be responsible for Identification, mapping and profiling of thought leaders of given geography and therapy area, on an ongoing basis. Roles & Responsibilities You will be responsible for the engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan You will be responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects You will be a therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients treatment trends and studies in the therapeutic areas in which the Company is involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart You will be responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals You will have to represent the organization in various internal & external scientific platforms You will have to gather deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams. You will need to proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan You will be receiving and processing scientific information requests received from physicians You will have to ensure that all activities in the region are conducted in alignment to organisation's COBE (Code of Business Ethics) Policy and compliance guidelines. You will need to collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in reputed journals. You will be responsible for devising an optimal training plan to ensure the flow of the latest medical developments to the sales and marketing teams. You will jointly be responsible with the therapy area lead to support optimal patient outcomes through communication of data, information, knowledge, and insights in support of healthcare professional needs and organizational goals. Representing the organization in various internal and external scientific platforms will be among your responsibilities. You will be responsible for developing the Medical Affairs strategic plan for identified therapeutic areas and products. Your ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest will be vital. You will be responsible for identifying knowledge gaps, practice gaps, and data gaps and developing strategic medical action plans, including but not limited to medical education, product education, evidence generation, and special projects, will fall under your responsibility. Collaborating with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, case series, patient-reported outcomes, and publishing them in reputable journals will be part of your role. Handling complex questions from healthcare professionals related to GGI products or disease areas to satisfaction will be a key responsibility. You will be responsible for ensuring that all activities in the therapeutic area are conducted in alignment with Dr. Reddy's COBE (Code of Business Ethics) Policy and compliance guidelines will be essential. You will be responsible for ensuring that all promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy's Promotional Material approval policy. As a product pipeline champion, you will have the ability to identify unmet needs through active stakeholder interactions and actively contribute to the new product ideation and development of differentiated products. Qualifications Educational Qualification- MBBS with full time post-graduate qualification of at least 2-years duration in any discipline of medicine/ M.B.B.S with M.B.A. from a reputed institute Minimum work experience- Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs. Skills & attributes Technical Skills Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship Experience with complex business environments preferred Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards. Behavioural Skills Integrity driven decision making skills Collaboration and teaming with ability to work in a matrix environment Strategic thinking & sound analytical skills Big picture orientation with attention to detail Sense of urgency & desire to excel Intellectual curiosity Self-awareness and adaptability Result oriented and performance driven Excellent interpersonal & communication skills to effectively interact with a broad range of audience.

We are looking for the Primary scientific face of the organization to Thought Leaders & physicians for a given therapy area. You will be responsible for Identification, mapping and profiling of thought leaders of given geography and therapy area, on an ongoing basis. Roles & Responsibilities You will be responsible for the engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan You will be responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects You will be a therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients treatment trends and studies in the therapeutic areas in which the Company is involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart You will be responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals You will have to represent the organization in various internal & external scientific platforms You will have to gather deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams. You will need to proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan You will be receiving and processing scientific information requests received from physicians You will have to ensure that all activities in the region are conducted in alignment to organisation's COBE (Code of Business Ethics) Policy and compliance guidelines. You will need to collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in reputed journals. You will be responsible for devising an optimal training plan to ensure the flow of the latest medical developments to the sales and marketing teams. You will jointly be responsible with the therapy area lead to support optimal patient outcomes through communication of data, information, knowledge, and insights in support of healthcare professional needs and organizational goals. Representing the organization in various internal and external scientific platforms will be among your responsibilities. You will be responsible for developing the Medical Affairs strategic plan for identified therapeutic areas and products. Your ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest will be vital. You will be responsible for identifying knowledge gaps, practice gaps, and data gaps and developing strategic medical action plans, including but not limited to medical education, product education, evidence generation, and special projects, will fall under your responsibility. Collaborating with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, case series, patient-reported outcomes, and publishing them in reputable journals will be part of your role. Handling complex questions from healthcare professionals related to GGI products or disease areas to satisfaction will be a key responsibility. You will be responsible for ensuring that all activities in the therapeutic area are conducted in alignment with Dr. Reddy's COBE (Code of Business Ethics) Policy and compliance guidelines will be essential. You will be responsible for ensuring that all promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy's Promotional Material approval policy. As a product pipeline champion, you will have the ability to identify unmet needs through active stakeholder interactions and actively contribute to the new product ideation and development of differentiated products. Qualifications Educational Qualification- MBBS with full time post-graduate qualification of at least 2-years duration in any discipline of medicine/ M.B.B.S with M.B.A. from a reputed institute Minimum work experience- Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs. Skills & attributes Technical Skills Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship Experience with complex business environments preferred Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards. Behavioural Skills Integrity driven decision making skills Collaboration and teaming with ability to work in a matrix environment Strategic thinking & sound analytical skills Big picture orientation with attention to detail Sense of urgency & desire to excel Intellectual curiosity Self-awareness and adaptability Result oriented and performance driven Excellent interpersonal & communication skills to effectively interact with a broad range of audience.

We are looking for the Primary scientific face of the organization to Thought Leaders & physicians for a given therapy area. You will be responsible for Identification, mapping and profiling of thought leaders of given geography and therapy area, on an ongoing basis. Roles & Responsibilities You will be responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals. You will have to represent the organization in various internal & external scientific platforms. You will have to gather deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams. You will need to proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan. You will be receiving and processing scientific information requests received from physicians. You will have to ensure that all activities in the region are conducted in alignment to organisation's COBE (Code of Business Ethics) Policy and compliance guidelines. You will need to collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in reputed journals. You will be responsible for devising an optimal training plan to ensure the flow of the latest medical developments to the sales and marketing teams. You will jointly be responsible with the therapy area lead to support optimal patient outcomes through communication of data, information, knowledge, and insights in support of healthcare professional needs and organizational goals. Representing the organization in various internal and external scientific platforms will be among your responsibilities. You will be responsible for developing the Medical Affairs strategic plan for identified therapeutic areas and products. Your ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest will be vital. You will be responsible for identifying knowledge gaps, practice gaps, and data gaps and developing strategic medical action plans, including but not limited to medical education, product education, evidence generation, and special projects, will fall under your responsibility. Collaborating with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, case series, patient-reported outcomes, and publishing them in reputable journals will be part of your role. Handling complex questions from healthcare professionals related to GGI products or disease areas to satisfaction will be a key responsibility. You will be responsible for ensuring that all activities in the therapeutic area are conducted in alignment with Dr. Reddy's COBE (Code of Business Ethics) Policy and compliance guidelines will be essential. You will be responsible for ensuring that all promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy's Promotional Material approval policy. As a product pipeline champion, you will have the ability to identify unmet needs through active stakeholder interactions and actively contribute to the new product ideation and development of differentiated products. Qualifications Educational Qualification MBBS with full time post-graduate qualification of at least 2-years duration in any discipline of medicine/ M.B.B.S with M.D from a reputed institute Minimum Work Experience Required Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs. Skills & Attributes Technical Skills Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship Experience with complex business environments preferred Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards Behavioural Skills Integrity-driven decision-making skills Collaboration and teaming with the ability to work in a matrix environment Strategic thinking & sound analytical skills Big picture orientation withattention to detail Sense of urgency & desire to excel Intellectual curiosity Self-awareness and adaptability Result-oriented and performance-driven Excellent interpersonal & communication skills to effectively interact with a broad range of audience

We are looking for the Primary scientific face of the organization to Thought Leaders & physicians for a given therapy area. You will be responsible for Identification, mapping and profiling of thought leaders of given geography and therapy area, on an ongoing basis. Roles & Responsibilities You will be responsible for the engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan You will be responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects You will be a therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients treatment trends and studies in the therapeutic areas in which the Company is involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart You will be responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals You will have to represent the organization in various internal & external scientific platforms You will have to gather deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams. You will need to proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan You will be receiving and processing scientific information requests received from physicians You will have to ensure that all activities in the region are conducted in alignment to organisation's COBE (Code of Business Ethics) Policy and compliance guidelines. You will need to collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in reputed journals. You will be responsible for devising an optimal training plan to ensure the flow of the latest medical developments to the sales and marketing teams. You will jointly be responsible with the therapy area lead to support optimal patient outcomes through communication of data, information, knowledge, and insights in support of healthcare professional needs and organizational goals. Representing the organization in various internal and external scientific platforms will be among your responsibilities. You will be responsible for developing the Medical Affairs strategic plan for identified therapeutic areas and products. Your ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest will be vital. You will be responsible for identifying knowledge gaps, practice gaps, and data gaps and developing strategic medical action plans, including but not limited to medical education, product education, evidence generation, and special projects, will fall under your responsibility. Collaborating with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, case series, patient-reported outcomes, and publishing them in reputable journals will be part of your role. Handling complex questions from healthcare professionals related to GGI products or disease areas to satisfaction will be a key responsibility. You will be responsible for ensuring that all activities in the therapeutic area are conducted in alignment with Dr. Reddy's COBE (Code of Business Ethics) Policy and compliance guidelines will be essential. You will be responsible for ensuring that all promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy's Promotional Material approval policy. As a product pipeline champion, you will have the ability to identify unmet needs through active stakeholder interactions and actively contribute to the new product ideation and development of differentiated products. Qualifications Educational Qualification- MBBS with full time post-graduate qualification of at least 2-years duration in any discipline of medicine/ M.B.B.S with M.B.A. from a reputed institute Minimum work experience- Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs. Skills & attributes Technical Skills Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship Experience with complex business environments preferred Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards. Behavioural Skills Integrity driven decision making skills Collaboration and teaming with ability to work in a matrix environment Strategic thinking & sound analytical skills Big picture orientation with attention to detail Sense of urgency & desire to excel Intellectual curiosity Self-awareness and adaptability Result oriented and performance driven Excellent interpersonal & communication skills to effectively interact with a broad range of audience.

We are looking for the Primary scientific face of the organization to Thought Leaders & physicians for a given therapy area. You will be responsible for Identification, mapping and profiling of thought leaders of given geography and therapy area, on an ongoing basis. Roles & Responsibilities You will be responsible for the engagement of identified key thought leaders through medical affairs activities, in alignment with the overall strategic plan? You will be responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects You will be a therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients treatment trends and studies in the therapeutic areas in which the Company is involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart? You will be responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals You will have to represent the organization in various internal & external scientific platforms You will have to gather deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams. You will need to proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan? You will be receiving and processing scientific information requests received from physicians? You will have to ensure that all activities in the region are conducted in alignment to organisation's COBE (Code of Business Ethics) Policy and compliance guidelines. You will need to collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in reputed journals. You will be responsible for devising an optimal training plan to ensure the flow of the latest medical developments to the sales and marketing teams. You will jointly be responsible with the therapy area lead to support optimal patient outcomes through communication of data, information, knowledge, and insights in support of healthcare professional needs and organizational goals. Representing the organization in various internal and external scientific platforms will be among your responsibilities. You will be responsible for developing the Medical Affairs strategic plan for identified therapeutic areas and products. Your ability to convert insights on disease trends and treatment patterns from key thought leaders into viable and formidable strategic plans to shape the therapeutic areas of interest will be vital. You will be responsible for identifying knowledge gaps, practice gaps, and data gaps and developing strategic medical action plans, including but not limited to medical education, product education, evidence generation, and special projects, will fall under your responsibility. Collaborating with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, case series, patient-reported outcomes, and publishing them in reputable journals will be part of your role. Handling complex questions from healthcare professionals related to GGI products or disease areas to satisfaction will be a key responsibility. You will be responsible for ensuring that all activities in the therapeutic area are conducted in alignment with Dr. Reddy's COBE (Code of Business Ethics) Policy and compliance guidelines will be essential. You will be responsible for ensuring that all promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with Dr. Reddy's Promotional Material approval policy. As a product pipeline champion, you will have the ability to identify unmet needs through active stakeholder interactions and actively contribute to the new product ideation and development of differentiated products. Qualifications Educational Qualification- MBBS with full time post-graduate qualification of at least 2-years duration in any discipline of medicine/ M.B.B.S with M.B.A. from a reputed institute Minimum work experience- Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs. Skills & attributes Technical Skills Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data? Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship? Experience with complex business environments preferred? Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards. Behavioural Skills Integrity driven decision making skills? Collaboration and teaming with ability to work in a matrix environment? Strategic thinking & sound analytical skills? Big picture orientation with attention to detail? Sense of urgency & desire to excel? Intellectual curiosity? Self-awareness and adaptability? Result oriented and performance driven? Excellent interpersonal & communication skills to effectively interact with a broad range of audience.

This job is with Johnson & Johnson, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. At Johnson & Johnson,?we believe health is everything. Our strength in healthcare innovation empowers us to build a?world where complex diseases are prevented, treated, and cured,?where treatments are smarter and less invasive, and?solutions are personal.?Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.?Learn more at https://www.jnj.com Job Function Medical Affairs Group Job Sub Function Medical Science Liaison Job Category Scientific/Technology All Job Posting Locations: Bangalore, Karnataka, India, Chennai, Tamil Nadu, India Job Description Job Description: Johnson & Johnson is recruiting for Medical Science Liaison- Oncology, Medical Affairs located in Bangalore, India. The position reports to the TA Lead - Oncology, Johnson & Johnson Innovative Medicine, India. Position Overview Be a therapeutic area scientific expert where you will be scientific face of the company engaging in interactions with Key Opinion Leaders(KOL) discussing treatment trends, clinical trial data of our molecules and seeking insights that support the medical strategy. Key Responsibilities Primary scientific face of the organization to KOL&aposs for Oncology therapy area, responsible for: Identification, mapping and profiling of KOL&aposs of the given geography and therapy area on an ongoing basis Engagement of identified KOL&aposs through medical affairs initiatives in alignment with the overall franchise plan Represent the TA for medical & scientific affairs on all relevant cross functional teams and internal and external initiatives. Gathering customer insights and conveying them back to the franchise team Receiving and processing scientific information request received from Healthcare Professionals(HCP) Scientific resource for the sales team of the given therapy area responsible for regular training and flow of latest medical developments in the given field This is a highly collaborative role that requires excellent communication and influencing skills with all internal stakeholders to develop and implement medical strategy, to shape the external scientific landscape that can enable the fastest access to new products/indications for our patients, medical staff and the greater community. The position will require 70-80% travel for interaction with customers and various stakeholders. Qualifications - External Medical graduate (MD/ MBBS/ BDS /MDS) or Pharmaceutical university Degree ( PharmD or PhD) Experience And Skills Minimum of 0-2 years' experience in pharmaceutical/healthcare industry Good understanding of medical affairs function Understanding of local regulatory policy and industry&aposs code of practice related to drug registration, pharmaceutical promotion and clinical research. Are you ready to impact the world Johnson & Johnson offers an unusual experience to professionals looking for an opportunity to work with hardworking people who share your real passion for caring in an environment that empowers you to drive your own career. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Show more Show less

As an Associate Director, Study Site Engagement at Takeda, you will play a key role in enhancing engagement and providing added value by establishing and nurturing long-term relationships with investigators and study site personnel. You will support study teams with trial operations from Feasibility through CSR within the assigned region or countries across Takeda therapeutic areas. Your responsibilities will include supporting country and site identification, feasibility, site selection, study recruitment strategies, and mitigating barriers at the direction of Clinical Programs. You will be responsible for Study Specific Engagement activities, such as early engagement for country and site feasibility, supporting the development of study site lists for feasibility, attending Pre-Study Visits, tracking start-up hurdles, supporting recruitment strategy and activities, and ensuring compliance with applicable local regulations and SOP trainings. Additionally, you will interact closely with local CRO teams throughout the lifecycle of the study and attend Investigator Meetings as required. In addition to study-specific activities, you may also be involved in Non-Study Specific Engagement activities, such as people management, establishing communication with regional/country Medical Affairs, and participating in SSE Program Lead and/or SSE Study Lead roles for assigned programs. You may also be responsible for developing and maintaining long-term strategic relationships with selected sites to improve the site and Takeda experience. To qualify for this role, you should have a scientific degree in pharmaceutical science, chemistry, biology, or healthcare, with 10+ years of experience in clinical research. You should have advanced knowledge of clinical trials processes, regulations, and ICH-GCP, as well as strong communication and influencing skills. Fluency in spoken and written English is required. This position is field-based with monthly visits to the Takeda Delhi/Mumbai office, and travel in the assigned region may be required up to 40% during busy periods. If you are looking for a patient-focused company that empowers its employees to work towards their potential and make a difference in the healthcare industry, Takeda could be the right place for you to take charge of your future and contribute to our inspiring mission of delivering Better Health and a Brighter Future to people around the world.,

We are seeking an influential professional for the Clinical Specialist Lead role within Spes Manning. You will be instrumental in developing and executing business plans for the Medical Aesthetics portfolio, providing internal and external training, and fostering strong relationships with key researchers and physicians. This role requires a strong medical background, experience in medical affairs within the pharmaceutical industry, and exceptional leadership and strategic thinking skills. Key Responsibilities: Business Planning: Work closely with Commercial leaders and the Associate Director, Medical Affairs, to set priorities and activities. Develop strategies and tactics for the Medical Aesthetics portfolio and implement/execute them in a timely manner to align with commercial strategies as budgeted. Develop and maintain awareness and understanding of competitor issues/intelligence. Contribute to the development of and maintain competitiveness and growth within the market and communicate intelligence to the commercial team as appropriate. Internal Training: Facilitate training to field sales teams and others to ensure up-to-date knowledge of Aesthetic products, relevant disease states, and conditions. Provide interpretation and perspective on competitor activities. Assist in the evaluation of sales team members skills and knowledge. Assist in the development of training materials, exams, and evaluative processes for field sales teams. External Training and Education: Through field visits, improve doctors awareness of Aesthetic products. Share scientific data supporting their use, train professionals in their proper use, and develop physician's expertise and comfort in prescribing their use. Work closely with the commercial team to facilitate training to physicians and provide proper engagement to thought leaders and doctors externally. Help shape the company's leadership image within the specialty area. Ensure the future success by identifying doctors-in-training with specialty interests which lie within the company's therapeutic range and fostering relationships through educational initiatives. Provide scientific and clinical information to Healthcare Professionals on request. Thought Leadership: Identify key researchers and physicians critical to the knowledge base and disease awareness relevant to the success of each of Aesthetic products in the specialty area. Facilitate greater understanding of medical practice patterns, educational, and training needs; organize local activities with the key stakeholders. Present and communicate Company's scientific perspective and vision at customer meetings; plan meeting agendas with key stakeholders; interpret feedback and results. Ensure the maintenance of key relationships with physicians and administrators of specialty societies. Phase IV trials/Clinical Studies: Identify and prioritize Phase IV and investigator-initiated study needs ; ensure that the approval process and execution of all Phase IV and IITs follow company guidelines and policies. Skills Required: Good leadership skills and able to persuade at all levels within the organization (including Commercial team) as well as with external customers (KOLs, HCPs, etc.). Ability to think strategically and develop and execute plans at country level. Good understanding of the domestic market. Experience in establishing strong influential relationships with KOLs. Good understanding of multinational culture and ways of working. Experience of working collaboratively and cross-functionally in a matrix structure, supporting multiple stakeholders. QUALIFICATIONS: Strong preference for medical degree (MD or MBBS).

We are seeking an influential professional for the Key Opinion Leaders role within Spes Manning. You will be instrumental in developing and executing business plans for the Medical Aesthetics portfolio, providing internal and external training, and fostering strong relationships with key researchers and physicians. This role requires a strong medical background, experience in medical affairs within the pharmaceutical industry, and exceptional leadership and strategic thinking skills. Key Responsibilities: Business Planning: Work closely with Commercial leaders and the Associate Director, Medical Affairs, to set priorities and activities. Develop strategies and tactics for the Medical Aesthetics portfolio and implement/execute them in a timely manner to align with commercial strategies as budgeted. Develop and maintain awareness and understanding of competitor issues/intelligence. Contribute to the development of and maintain competitiveness and growth within the market and communicate intelligence to the commercial team as appropriate. Internal Training: Facilitate training to field sales teams and others to ensure up-to-date knowledge of Aesthetic products, relevant disease states, and conditions. Provide interpretation and perspective on competitor activities. Assist in the evaluation of sales team members skills and knowledge. Assist in the development of training materials, exams, and evaluative processes for field sales teams. External Training and Education: Through field visits, improve doctors awareness of Aesthetic products. Share scientific data supporting their use, train professionals in their proper use, and develop physician's expertise and comfort in prescribing their use. Work closely with the commercial team to facilitate training to physicians and provide proper engagement to thought leaders and doctors externally. Help shape the company's leadership image within the specialty area. Ensure the future success by identifying doctors-in-training with specialty interests which lie within the company's therapeutic range and fostering relationships through educational initiatives. Provide scientific and clinical information to Healthcare Professionals on request. Thought Leadership: Identify key researchers and physicians critical to the knowledge base and disease awareness relevant to the success of each of Aesthetic products in the specialty area. Facilitate greater understanding of medical practice patterns, educational, and training needs; organize local activities with the key stakeholders. Present and communicate Company's scientific perspective and vision at customer meetings; plan meeting agendas with key stakeholders; interpret feedback and results. Ensure the maintenance of key relationships with physicians and administrators of specialty societies. Phase IV trials/Clinical Studies: Identify and prioritize Phase IV and investigator-initiated study needs ; ensure that the approval process and execution of all Phase IV and IITs follow company guidelines and policies. Skills Required: Good leadership skills and able to persuade at all levels within the organization (including Commercial team) as well as with external customers (KOLs, HCPs, etc.). Ability to think strategically and develop and execute plans at country level. Good understanding of the domestic market. Experience in establishing strong influential relationships with KOLs. Good understanding of multinational culture and ways of working. Experience of working collaboratively and cross-functionally in a matrix structure, supporting multiple stakeholders. QUALIFICATIONS: Strong preference for medical degree (MD or MBBS).

Are you an experienced medical professional passionate about Medical Affairs Do you thrive in a dynamic environment and enjoy implementing medical affairs strategies Novo Nordisk India Private Limited is looking for a Regional Medical Advisor to join their Semaglutide North department. In this role, you will actively contribute to medico-marketing activities and support the implementation of the Medical Affairs strategy in the country. Your responsibilities will include: - Executing the Indian medical strategy in your designated region. - Building and maintaining strong scientific relationships with key influencers and stakeholders. - Conducting training and educational activities for Physicians and other Health Care Professionals (HCPs) specializing in diabetes and obesity. - Providing medical support to the brand team. - Assisting the marketing and sales team in developing product and promotional strategies, anticipating market challenges, and taking timely actions. - Keeping updated on scientific knowledge through participation in scientific meetings, gathering insights from key opinion leaders, and communicating with internal stakeholders. - Educating and training field and marketing personnel on disease, product, and therapy aspects relevant to the promotional strategy. - Establishing a strong advocacy of Novo Nordisk's portfolio with key external stakeholders through ongoing scientific interactions. To qualify for this position, you should hold an MBBS/MD in Pharmacology from a reputed institution. Strong scientific knowledge and interest in diabetes and obesity, collaboration skills, communication abilities, and analytical capabilities are essential. Additionally, skills in planning, execution, and follow-up, along with a creative and innovative attitude, are required to excel in this role. The Clinical, Medical, and Regulatory (CMR) department at Novo Nordisk is known for its diversity and collaboration. From interactions with healthcare professionals to regulatory strategies and medical education, CMR plays a crucial role in supporting Novo Nordisk's products with a patient-centered focus. At Novo Nordisk, every day is dedicated to finding solutions for defeating serious chronic diseases. The company values an unconventional spirit, determination, and curiosity in approaching work. With a focus on improving patients" quality of life through innovative solutions, Novo Nordisk is committed to making a difference in healthcare. If you are ready to contribute to Novo Nordisk's mission, apply by submitting your CV and motivational letter online before the deadline on 12/08/2025. Internal candidates are advised to inform their line Managers before applying. Novo Nordisk emphasizes an inclusive recruitment process and equal opportunities for all job applicants. The company does not extend unsolicited employment offers or charge fees to prospective employees during the recruitment process. Join Novo Nordisk in shaping the future of healthcare with an unordinary approach that drives real, lasting change in health.,

URGENT HIRING !!! location's : Canada , Australia , New Zealand ( Not In India ) Benefits : Medical Insurances , Travel allowances , Flight Tickets , Meals , etc For more information call or whatsapp +91 9220850077 Key Responsibilities: Diagnose and treat common illnesses and injuries. Conduct routine check-ups, medical tests, and health assessments. Prescribe medications and recommend treatment plans. Provide preventive healthcare advice and patient education. Refer patients to specialists when necessary. Assess and monitor patient conditions. Administer medications and injections as prescribed. Assist doctors in medical procedures and surgeries. Provide emotional support to patients and families. Maintain accurate medical records and follow safety protocols.

Summary In line with overall product strategy, the Medical Lead is responsible for supporting the design, implementation and execution of Medical Affairs plans for assigned Therapy Area, providing scientific information, helping design & organize clinical studies, building educational dialogue with KOLs and regulatory stakeholders About The Role Key Responsibilities Support country medical affairs strategy in line with the global strategy, country insights and market conditions, and implementation of Medical Affairs activities within the designated therapy area(s), Coordinate scientific meeting, symposia, congresses, Continuous Medical Education (CME) and other medical / scientific exchange and engagement activities which could bring value to the therapy area; develop engagement plan(s) for country customer-facing activities and events, and ensure timely execution of the activities in an efficient and compliant way, Ensure enquiries are responded to in a quality, timely manner, and in accordance with applicable standards; establish response documents for frequently asked questions, Provide medical/scientific input into the development and execution of clinical trial or clinical research related activities, including initiation and oversight of clinical studies / clinical research within the therapeutic area Support country strategy for Non Interventional Studies/Investigator Initiated Trial activities, Coordinate review and approval of medical materials and locally developed promotional materials; ensure medical materials provided from global or region for partner engagement and events are tailored to local needs, and reviewed/approved per local/P3 guidelines, Ensure medical insights are provided to cross-functional groups, including, but not restricted to: Pharmacovigilance, Regulatory Affairs, Market Access, QA, Commercial and Brand team and others, Responsible for risk identification and assessment, mitigation planning as well as implementation and monitoring of appropriate internal controls within the area of responsibilities Essential Requirements MBBS; MD Mandatory with min 2+ year industry experience Operations Management and Execution Project Management Collaborating across boundaries Clinical Trial Design, Data & Reporting Medical Science and Disease Area Knowledge Medical Education and Scientific Engagement Non-Interventional Studies (NIS) / Epidemiology Studies Medical Governance and Medical Safety Desirable Requirements: Ophthalmology &/or immunology Why Novartis: Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and trusted medicines company in the world How can we achieve thisWith our people It is our associates that drive us each day to reach our ambitions Be a part of this mission and join us! Learn more here: https:// novartis / about / strategy / people-and-culture Youll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook https:// novartis /careers/benefits-rewards Commitment To Diversity And Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve, Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl india@novartis and let us know the nature of your request and your contact information, Please include the job requisition number in your message, Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork novartis /network Why Novartis: Helping people with disease and their families takes more than innovative science It takes a community of smart, passionate people like you Collaborating, supporting and inspiring each other Combining to achieve breakthroughs that change patientslives Ready to create a brighter future togetherhttps:// novartis / about / strategy / people-and-culture Join our Novartis Network: Not the right Novartis role for youSign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork novartis /network Benefits and Rewards: Read our handbook to learn about all the ways well help you thrive personally and professionally: https:// novartis /careers/benefits-rewards Show

Essential Functions: Work as a Product Manager/Executive within the Ophthalmology division, leveraging sales experience to drive brand success. Proactively plan and strategize by identifying emerging market trends and aligning them with company goals. Design promotional and communication strategies for various brands. Plan and execute customer-centric campaigns and special initiatives for priority products. Execute campaign strategies for Key Opinion Leaders (KOLs). Conduct monthly and quarterly brand reviews to monitor and evaluate performance. Perform regular fieldwork to assess the implementation of marketing strategies. Coordinate with cross-functional support teams for smooth execution of marketing plans. Manage budgets, resource allocation, and sampling for assigned brands. Address and resolve field queries in a timely manner. Additional Responsibilities: Work closely with sales teams to provide product training and support. Monitor competitor activities and market dynamics to adapt strategies. Collaborate with Medical Affairs for evidence generation and promotional compliance. Drive digital initiatives aligned with brand strategy

Accounts Receivable Coord I Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business-critical services that support our business. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life . Discover what our 29,000 employees, across 110 countries already know. Why Syneos Health We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. WhyBecause when we bring together diversity of thoughts, backgrounds, cultures, and perspectives we re able to create a place where everyone feels like they belong. Job Responsibilities Duties & Responsibilities: Prepare invoice package from consolidated monthly data file. This includes preparing pivot tables and compiling scanned image backup. Route prepared invoice packages to Project Managers for review and approval Generate pass through invoices in Oracle. Create invoice pdf package and save invoices, summary and backup scans to M drive Email PDF invoice package to clients or send hard copies via Federal Express if originals are needed Update the Billing Repository after invoices are created, costs are checked, and invoice number is added to the repository Respond to invoice related questions from operations or clients Generate investigator invoices in Oracle and send to client Provide Billing supervisor with details of corrections which require a journal to be prepared, they could be for: - Project to project recode - Costs which cannot be recharged following PM approval Update the Billing Repository for the above changes Process credits and rebills as required Requirements: 1 3 years of experience in invoicing and cash application Knowledge of invoice generation and credit memo processing Strong written and verbal communication skills Strong Excel skills at least intermediate level, any ERP system experience Experience of working in a multi-currency environment Good organizational skills Ability to communicate well when working with colleagues/clients in other countries Attention to detail and accuracy Desirable: Experience of using Oracle ERP system Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Role & responsibilities Experienced professional individual contributor that works under limited supervision. Applies subject matter knowledge in the area of Medical Affairs. Requires capacity to apply skills/knowledge within the context of specific needs or requirements MAIN RESPONSIBILITIES As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities. Contributes to implementation of clinical protocols, and facilitates completion of final reports. Recruits clinical investigators and negotiates study design and costs. Responsible for directing human clinical trials, phases III & IV for company products under development. Participates in adverse event reporting and safety responsibilities monitoring. Coordinates and provides reporting information for reports submitted to the regulatory agencies. Monitors adherence to protocols and determines study completion. Coordinates and oversees investigator initiations and group studies. May participate in adverse event reporting and safety responsibilities monitoring. May act as consultant/liaison with other corporations when working under licensing agreements. QUALIFICATIONS MD Pharmacology Field Work 15 days in a month

Decision Analytics Consultant - MLR Review (Medical, Legal, and Regulatory) The Consultant for MLR Review in the DCE Marketing Services team is a critical member responsible for overseeing the review and approval of promotional and non-promotional materials. This role demands expertise in the end-to-end Medical, Legal, and Regulatory (MLR) review and submission processes, ensuring compliance with external regulations, industry standards (EFPIA/IFPMA), and company policies. The Consultant collaborates with cross-functional teams to provide regulatory guidance and streamline operations across the MLR landscape. What Youll Do Compliance Advisory: Serve as the lead compliance advisor for designated therapy areas, ensuring all promotional and non-promotional content complies with global standards, including disease awareness and scientific communications. MLR Review Oversight: Manage the full MLR (Medical, Legal, Regulatory) review cycle, guaranteeing timely, accurate submissions and approvals in line with regulatory requirements. Expert Guidance: Provide subject matter expertise across MLR processes, including documentation, workflow systems, and cross-functional collaboration. Strategic Input: Offer compliance-focused strategic input during concept reviews to align content development with both business objectives and regulatory standards. Training & Enablement: Lead training initiatives on MLR systems and compliance for internal stakeholders across functions such as sales, marketing, and medical affairs. Global Collaboration: Work closely with country affiliates to support material approvals, resolve compliance issues, and share best practices across regions. Labeling Compliance: Keep stakeholders updated on EU labeling changes and assess their impact on promotional and non-promotional material content. What Youll Bring 7-10 years of experience in regulatory, medical affairs, or healthcare compliance, with a strong focus on MLR review processes. Expertise in global standards for advertising and promotion, including EFPIA/IFPMA codes and ABPI Code of Practice. Familiarity with regulatory bodies such as the Medicines and Healthcare products Regulatory Agency (MHRA) and their compliance expectations. Thorough understanding of the MLR review and submission process, including workflows, approvals, and stakeholder management. Ability to effectively communicate regulatory requirements and provide strategic guidance to cross-functional teams. Strong organizational skills with the ability to manage multiple priorities and meet deadlines in a fast-paced environment. This Consultant role offers a dynamic opportunity to ensure compliant and efficient MLR operations while supporting strategic business objectives across the pharmaceutical marketing landscape.

Role & responsibilities : Excellent Medical Writing Skills Excellent interpersonal and communication skills Should be proficient in word /PowerPoint and excel Will be expected to Support sales force trainings, present science news, activity plans etc. Candidate should address scientific queries received from sales/marketing/doctors with sound scientific back-up Should possess ability to present scientific content at academic meets like CMEs, conferences, advisory boards etc. Provide pre-launch and launch training to sales staff for new products Approval of promotional inputs as per regulatory guidelines/pharma marketing codes Involvement in strategies and planning for launch of new indication/products including KOL engagement and medical education. Building a professional rapport with Key Opinion Leaders through field visits Liaison with KOLs to build and drive scientific advocacy for the product/therapy area Candidate will devise phase 4 post-marketing studies incl. registries, RWE, observational studies Should be aware of Pharmacovigilance process and adverse event reporting. Candidate will collaborate with the marketing department to develop marketing strategies Provide inputs in new product evaluation and product pipeline for future launch Travel for Cycle meetings, Conference participation and other medico-marketing activity Preferred candidate profile : MBBS, MD Pharmacology/medicine Candidate should be from well recognized Reputed Govt Institute. Perks and benefits : Interested candidates can share their cv with purnima.chauhan@walterbushnell.com

The main purpose of your role as an experienced professional individual contributor in Medical Affairs is to work under limited supervision and apply your subject matter knowledge effectively. Your capacity to apply skills and knowledge should meet specific needs or requirements within the field. As an experienced professional in the Medical Affairs Sub-Function, you will be responsible for overseeing the direction, planning, and execution of clinical trials and research activities. You will play a key role in data collection, implementation of clinical protocols, and ensuring completion of final reports. Additionally, you will be involved in recruiting clinical investigators, negotiating study designs and costs, and directing human clinical trials, specifically phases III & IV for company products under development. Your responsibilities will also include participating in adverse event reporting, safety responsibilities monitoring, coordinating reporting information for submissions to regulatory agencies, monitoring adherence to protocols, and determining study completion. Furthermore, you will coordinate and oversee investigator initiations and group studies. You may also act as a consultant or liaison with other corporations when working under licensing agreements. In terms of education, you are required to have an Associates Degree (13 years), and a minimum of 1 year of relevant experience in the field. Your role demands a high level of professionalism, attention to detail, and the ability to work effectively within a team environment to achieve the goals of the Medical Affairs Sub-Function.,