108 Clinical Jobs

Note: This role would involve Rotational Shifts (Morning and Nights) Basic roles: Patient care Maintain compliance Clinically sound Assist the surgeon/Consultant Roles and Responsibilities Basic roles: Patient care Maintain compliance Clinically sound Assist the surgeons

Role Proficiency: 4 to 7years of Overall testing experience. Test Automation Experience with the tool Selenium or Katalon. Should have experience in Test Automation Framework like TestNG and Cucumber Framework. Able to manage test activities in large projects. Demonstrates appropriate interpersonal skills required to establish effective working relationships with clients and/or business partners. Should be familiar with the Software Testing tools, techniques and market trends. Should review user and functional requirements and provide feedback; they will Informally test early versions of functionality and develop increasingly complete test scripts and traceability; Participate in test execution and monitor the progress of execution. Proactively engage with all team members including developers, business users and business analysts. Writes, reviews and executes formal test scripts including setup and data requirements, procedures and expected results. Able to provide direct input to project estimates and documentation (Project Plan document, URS, FRS, Design docs) Reviews project requirements, plans and prototypes and providing input. Agile/ Scrum experience. Katalon Tool knowledge is preferable. Clinical domain knowledge is preferable Required Skills Selenium,kalaton,Cucumber Framework,Agile Scrum

Job Type- Fresher or Internship level Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. Responsibilities: 1. Assist in Protocol Development: Collaborate with the clinical research team to contribute to the development and review of clinical trial protocols. 2. Site Identification and Selection: Participate in the process of identifying and selecting clinical trial sites by conducting feasibility assessments. 3. Regulatory Compliance: Support the team in ensuring regulatory compliance throughout the clinical trial process. Assist in the preparation and submission of regulatory documents to appropriate health authorities. 4. Site Initiation: Assist in the initiation of clinical trial sites by coordinating site training activities and ensuring that all necessary documentation is in place. 5. Monitoring and Data Collection: Work closely with clinical research associates and investigators to monitor and collect data during the clinical trial. Assist in ensuring data accuracy, completeness, and adherence to protocol. 6. Adverse Event Reporting: Contribute to the process of monitoring and reporting adverse events, ensuring compliance with regulatory requirements. 7. Study Close-Out: Participate in the close-out activities of clinical trials, including the collection of essential documents and finalizing study reports. 8. Collaboration and Communication: Work collaboratively with cross-functional teams, including clinical operations, data management, and regulatory affairs. Communicate effectively with investigators, site staff, and study sponsors. 9. Documentation and Record Keeping: Maintain accurate and up-to-date documentation of all activities performed during the internship. Contribute to the development and organization of the trial master file. 10. Learning and Development: Actively engage in learning opportunities provided during the internship to enhance knowledge of clinical research processes and industry regulations. Qualifications: Currently enrolled in a Bachelor's or Master's degree program in a related field (e.g., Life Sciences, Pharmacy, Nursing, etc.). Excellent communication and interpersonal skills. Detail-oriented with strong organizational and time management abilities. Ability to work independently and as part of a team.

Job Description: The Clinical Pharmacist at Manipal Hospitals will be responsible for optimizing patient medication therapy to ensure safe and effective pharmaceutical care. The role includes conducting medication reviews, collaborating with healthcare professionals to develop therapeutic plans, and ensuring adherence to clinical guidelines and policies. The Clinical Pharmacist will also provide pharmacotherapy consultations, educate patients and healthcare staff regarding medication use, and participate in clinical rounds to monitor patient progress. Roles and Responsibilities Key Responsibilities: - Review and interpret medication orders to ensure appropriateness, safety, and efficacy. - Collaborate with physicians, nurses, and other healthcare professionals to develop and manage pharmaceutical care plans. - Conduct medication reconciliation and provide education to patients regarding their medications. - Monitor and evaluate patients for drug therapy outcomes, side effects, and drug interactions. - Participate in clinical rounds and provide input on medication-related issues. - Develop and implement policies and procedures relating to medication management. - Provide training and guidance to pharmacy staff and other healthcare professionals. - Stay updated with the latest research and developments in pharmacotherapy.

Role & responsibilities Education: MBBS (Bachelor of Medicine, Bachelor of Surgery) degree from a recognized medical school. Need a TS Registration. Work Environment: The Wellness MBBS Doctor may work in a wellness clinic, health center, private practice, corporate health programs, or integrated medical centers. They may be required to interact with diverse patient populations, providing individualized care plans to support long-term health goals. Fresher, clinical or wellness setting is preferred. Skills: Strong communication skills to engage and educate patients. Knowledge in nutrition, exercise, and mental health strategies. Ability to work in a team-oriented environment. Only female can apply. Compassionate, empathetic, and patient-focused approach. Female Doctor can apply. Schedule : Rotational shift Location : Kondapur

Role & responsibilities Education: MBBS (Bachelor of Medicine, Bachelor of Surgery) degree from a recognized medical school. Need a AP Registration. Work Environment: The Wellness MBBS Doctor may work in a wellness clinic, health center, private practice, corporate health programs, or integrated medical centers. They may be required to interact with diverse patient populations, providing individualized care plans to support long-term health goals. Fresher, clinical or wellness setting is preferred. Skills: Strong communication skills to engage and educate patients. Knowledge in nutrition, exercise, and mental health strategies. Ability to work in a team-oriented environment. Only female can apply. Compassionate, empathetic, and patient-focused approach. Female Doctor can apply. Schedule : Rotational shift Location :Vijayawada & Tirupati

Role & responsibilities Looking for candidate who focus specifically on the pharma and healthcare sector, such as those specializing in pharmaceutical domain terminologies & functions. Min 3 years experience is required. 2-8 years in pharmaceutical or healthcare recruitment This is a permanent work from home. Interested candidates can send their CV on alka.p@peoplesource.in Immediate joiners will be preferred. Alka Pathak Tiwari Senior Recruitment Consultant (M) - +91 8720862919 Email: alka.p@peoplesource.in

Responsibilities: Diagnose eye diseases using clinical techniques Prescribe medication and contact lenses as needed Perform refractions and eye exams low vision and vision therapy plans Handling of the individual OPD vision center Patient counselling Sales incentives Annual bonus Performance bonus Retention bonus Leave encashment

Greetings from HCL! Currently Hiring for "Paragon" JD: Paragon EHR Solution Expertise System Configuration User Support Quality Assurance & Data Integrity Workflow Analysis Documentation Training Development Reporting and Analysis Compliance and Regulatory Knowledge Collaboration & Communication Problem-Solving & Analytical Skills Experience with Older EHR Versions Familiarity with Additional EHR Platforms Customer Service Orientation Experience - 3-14 years Location - Bangalore / Chennai / Noida / Pune / Hyderabad Notice period - Immediate to 30 days Only CTC - Can be discussed Interested candidate please share below details along with update resume Candidate Name- contact Number- Email ID- Total Experience- Relevant Experience- Current company- Preferred location- Notice Period- Current CTC- Expected CTC- Interested candidate please drop mail to "kushmathattanda.baby@hcltech.com" Regards, Kushma kushmathattanda.baby@hcltech.com

Greetings from HCL! Currently Hiring for "NextGen" JD: NextGen EHR Knowledge System Configuration User Support Quality Assurance Workflow Analysis Compliance and Regulatory Oversight Technical or Healthcare Degree Communication Skills Problem-Solving Abilities Clinical Workflow Knowledge Older Version of NextGen Additional EHR Modules Customer Service Orientation Adaptability to New Technologies Experience - 3-15 years Location - Bangalore / Chennai / Noida / Pune / Hyderabad Notice period - Immediate to 30 days Only CTC - Can be discussed Interested candidate please share below details along with update resume Candidate Name- contact Number- Email ID- Total Experience- Relevant Experience- Current company- Preferred location- Notice Period- Current CTC- Expected CTC- Interested candidate please drop mail to "kushmathattanda.baby@hcltech.com" Regards, Kushma kushmathattanda.baby@hcltech.com

Greetings from HCL! Currently Hiring for "Altera Allscripts" JD: S Evaluation Focus Ability to customize and configure Allscripts EHR for specific healthcare needs Experience in delivering frontline support and training to clinical staff Skills in maintaining data integrity and ensuring data accuracy Capability to analyze and streamline EHR workflows with healthcare providers Proficiency in maintaining detailed system configuration records Experience in developing and conducting training sessions for system users Ability to generate and analyze reports for system performance improvement Knowledge of healthcare regulations like HIPAA, ensuring system compliance Skills in working with healthcare providers, administrators, and IT teams Experience in identifying and troubleshooting system issues Possession of a degree in technology, healthcare informatics, or related field 10-12 years of relevant experience in Allscripts EHR Solutions Demonstrated expertise in three or more Allscripts modules Strong understanding of clinical workflows and healthcare operations Excellent communication and interpersonal skills Proficiency in problem-solving and analytical thinking Familiarity with healthcare regulations and compliance, including HIPAA Experience with older versions of Allscripts EHR Familiarity with additional EHR platforms or healthcare IT systems Customer service orientation with a proactive approach to client engagement Experience - 3-12 years Location - Bangalore / Chennai / Noida / Pune / Hyderabad Notice period - Immediate to 30 days Only CTC - Can be discussed Interested candidate please share below details along with update resume Candidate Name- contact Number- Email ID- Total Experience- Relevant Experience- Current company- Preferred location- Notice Period- Current CTC- Expected CTC- Interested candidate please drop mail to "kushmathattanda.baby@hcltech.com" Regards, Kushma kushmathattanda.baby@hcltech.com

Greetings from HCL! Currently Hiring for "Meditech" JD: Meditech Expanse EHR Knowledge System Configuration User Support Quality Assurance Workflow Analysis Documentation Reporting and Analysis Compliance and Regulatory Oversight Communication and Interpersonal Skills Problem-solving and Analytical Abilities Technical Bachelor™s Degree or Related Field Experience with Older Versions of Meditech EHR Additional Meditech Modules Familiarity Eagerness to Learn and Adapt Customer Service Orientation Experience - 3-12 years Location - Bangalore / Chennai / Noida / Pune / Hyderabad Notice period - Immediate to 30 days Only CTC - Can be discussed Interested candidate please share below details along with update resume Candidate Name- contact Number- Email ID- Total Experience- Relevant Experience- Current company- Preferred location- Notice Period- Current CTC- Expected CTC- Interested candidate please drop mail to "kushmathattanda.baby@hcltech.com" Regards, Kushma kushmathattanda.baby@hcltech.com

Title The Software Development Manager is a vital position in our organization as we grow our software development environment and expand our IT department in Mumbai. Our Software Development department delivers solutions that enable and empower both internal and external customers to manage their business processes most effectively and efficiently. This individual will be tasked with accelerating the modernization of Medpace clinical and administrative software. Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across almost 40 countries. Responsibilities Manage software engineers and software development projects to implement effective and high-quality software solutions; Collect, analyze, and document user requirements; Perform project management, ensure system quality and oversee content management; Coordinate with company-wide leadership regarding software development projects; Design, modify, develop, support, install, and document software applications; Participate in software quality control and validation processes through development, code review, and/or execution of test plan/cases/scripts; Train software engineers and end users; and Identify process deficiencies and propose improvements. Qualifications Bachelor's Degree in Computer Science or a related area, with eight years of software development and three years of project lead experience; Prior experience in project management, execution, and delivery to customers, and in direct management of a development team; Development Experience with Microsoft technologies such as .NET and SQL Server; Development Experience in web based technologies such as Angular; Excellent analytical, written and oral communication skills in English; Knowledge of Azure and SharePoint technologies preferred; and Experience in a clinical (or regulated) environment is a plus! People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Medical Officer – Clinical assessment of the patients' medical/health problems by referring to their history and carrying out diagnosis, investigation, treatment for the stipulated period of time as mentioned. Provide Maternal, Newborn Child & Adolescent Healthcare including identification of high-risk pregnancies & appropriate referral. Proper counseling for quick referral, regular intake of medicines. Maintain confidentiality and impartiality of patients. Effective functioning of MHC, supervision of other staff functions. Reach & Leave timely from FSDP. Counsel patients about their illness or disease. Counsel patients about the dietary requirements as per their illness. Motivate them to have healthy and hygienic lifestyle. Take appropriate action for Bio Medical Waste Management with other staff. Counsel the patient about various communicable and non-communicable diseases. Counsel the patient about to preventive and curative measures of various seasonal, water and airborne diseases. Update to pharmacist about the medicinal requirement from time to time. Coordinate to paramedical team for insure their responsibilities. Submission of the monthly time sheet to Project Coordinator timely. Preparing the medicine indent and submitting it to the concern authority well in advance to avoid the scarcity of medicines. Any other task as assigned by Reporting Manager. MBBS Teamwork Proactive

Job Title: Optometrist Location: Yelahanka Company Name: Manipal Hospitals Job Description: We are seeking a qualified and dedicated Optometrist to join our team at Manipal Hospitals in Yelahanka. The successful candidate will be responsible for providing comprehensive eye examinations, diagnosing vision problems, and prescribing corrective lenses. The Optometrist will also educate patients on eye health and assist in the management of various ocular conditions. The ideal candidate will have a strong commitment to patient care and the ability to work collaboratively with other healthcare professionals. Key Responsibilities: - Conduct thorough eye examinations and vision tests - Diagnose refractive errors and ocular diseases - Prescribe glasses, contact lenses, and other visual aids - Provide patient education on eye health, preventive care, and treatment options - Maintain accurate patient records and documentation - Collaborate with ophthalmologists and other healthcare staff to ensure comprehensive patient care - Stay updated on advancements in optometry and eye care practices Skills and Qualifications: - Bachelor’s or Master’s degree in Optometry from an accredited institution - Valid optometry license to practice in the respective state - Strong clinical skills and knowledge of eye care practices - Excellent communication and interpersonal skills - Ability to work effectively in a team-oriented environment - Strong attention to detail and problem-solving abilities - Familiarity with optometric equipment and technology Tools and Equipment Required: - Ophthalmoscope and retinoscope - Autorefractor and lensometer - Visual field testing equipment - Optical coherence tomography (OCT) machines - Digital imaging systems Candidates who meet the qualifications and are passionate about providing exceptional eye care are encouraged to apply. Join us at Manipal Hospitals to make a positive impact on the lives of individuals in the Yelahanka community. Roles and Responsibilities **About the Role:** As an Optometrist at Manipal Hospitals Yelahanka, you will play a critical role in providing high-quality eye care services to patients. Your primary responsibilities will include conducting comprehensive eye examinations, diagnosing visual conditions, and recommending appropriate corrective measures. You will also be expected to stay updated on the latest advancements in optometry to ensure the best patient outcomes. **About the Team:** You will be part of a dynamic and multidisciplinary team dedicated to promoting eye health and providing exceptional patient care. The optometry team collaborates closely with ophthalmologists, nurses, and clinical support staff to deliver integrated eye care services. The team emphasizes a patient-centered approach, fostering an environment of teamwork and mutual respect. **You are Responsible for:** - Conducting detailed eye exams and assessments to evaluate patients’ visual acuity and ocular health. - Diagnosing eye conditions and recommending treatment plans, including glasses, contact lenses, and referral to specialists when necessary. - Educating patients about eye health, preventive care, and the importance of regular eye examinations. - Maintaining accurate patient records and ensuring compliance with healthcare regulations and standards. **To succeed in this role – you should have the following:** - A valid optometry degree and current licensure to practice as an optometrist. - Strong clinical skills and the ability to diagnose and manage various ocular conditions. - Excellent communication and interpersonal skills to effectively interact with patients and team members. - A commitment to continuous learning and staying informed about advances in optometry and best practices in patient care.

Greetings From Access Healthcare!! ! Need freshers with Life Science / Para- medical / Ancillary Medical courses Applicable only to candidates with strong knowledge in Human Anatomy and Physiology. Candidates must be prepared on 11 systems in Anatomy and physiology/Medical terminology/abbreviations/patho-physiology - Curriculum Candidates with certification will be preferred most. Work location: Chennai (Ambattur IE) Work mode: Work from office Interview Mode: Face to Face Walk-in Venue : Access Healthcare Headquarters, A9, 1st Main Road, Ambattur Industrial Estate, Chennai - 600058 Interview date and timing: 19, 20 & 21st June 2025, 10.30 AM onwards Looking for immediate Joiners. Shift: Day Shift All Must Bring Updated Resume With Aadhar Card contact praveen 9655581000 only watsapp praveen.t@accesshealthcare.com

Greetings from Sunrise Biztech Systems..!! Job Description: Position: Jr./Sr. Pharma Recruiter - US Staffing Location: Manyata Tech Park - Bangalore, KA INDIA (Onsite Only) Experience: 2-5yrs of US Staffing Experience Please share your updated CV at careers@sunrisesys.com Roles & Responsibilities Proactively source, screen, identify & qualify the best suitable candidate for client requirements. Should have excellent communication skills, Good interpersonal and team coordination skills. Effectively manage multiple job requisitions and deliver on a high volumes. Require active co-ordination with business accounts and efficiency in feedback management. Should be well versed with Tax terms (Mandatorily working with W2) , Should have worked with direct clients only (VISAs GC holder & US Citizen) Preferred Qualifications & Skills: Working experience in US Pharma accounts Working on Core scientific, Clinical & Admin requirements Experience in delivering clinical, professional and engineering placements. Working with MSP/VMS accounts is mandatory. Meeting targets and SLAs on daily/weekly/quarterly basis Perks and Benefits: # Competitive Compensation # Multiple Level Incentives # Rewards & Bonus # Free Transport (Pickup & Drop) # Free Food (Snacks & Dinner) # Health Insurance & Accidental Insurance Sunrise Biztech Systems - A trusted name among Fortune 500 Companies and Government agencies across the United States of America. Be part of an awesome company certified by Great Place to Work (5 consecutive times 2021-2025). Be incredibly successful in your work and continue to learn the latest recruitment skills and technology tools.

Location : Vijayawada , Andhra Pradesh Office timings : 1:30 Pm to 10 PM Client details : Channelsoft IT services Pvt Ltd Domain: Health Care (Clinical Trails) About Channelsoft Channel Soft is a pioneer in IT outsourcing and offshore software development business that envisioned and instigated the adoption of the flexible business practices that today enable our client companies to operate more efficiently and produce more value. Currently in India we have employees around 550+ working on various technologies like java,.net , DB, BI, AWS and support team . Office address : Nagarjuna nagar , near NTR university , Vijayawada . Responsibilities For Clinical SAS Programmer: Creating and executing SAS edit check programs Validating edit check programs using standard validation practices and processes Creating, validating and executing SAS programs and macros Utilizing SAS programming skills to provide ad-hoc reports (external and internal) and participating in project meetings (internal and external) Assist in developing programming specifications and in creating program specific validation plans Identifying and implementing solutions for complex reporting needs Creating and/or reviewing data editing and export specifications Working directly with clinical data manager and where needed with clinical project manager and other team members to ensure specifications are clear and accurate. Has a clear understanding of the contextual requirements for reporting outputs; and provides feedback Programming data cleaning/consistency checking programs to support internal applications for all therapeutic areas Programming and testing data export programs in accordance with specific client needs Documenting all programming and validation efforts in accordance with Good Clinical Practices Monitoring data integrity throughout a given study and utilizing SDTM guidelines to create transfer datasets Participating in the development of data editing conventions, specification documents and Clinical Data Management (CDM) processes Contributing to, designing and maintaining a library of reusable code Leading and managing enhancements to current CDM systems and providing inputs in the implementation of new systems Working independently and efficiently with minimal input required from the manager. Reviewing timelines; and projecting estimates and target dates in conjunction with direct supervisor and project team Adhering to target dates for project timelines and communicating any changes in target date to appropriate personnel including Project Manager Keeping department head informed of progress as well as potential impediments Adhering to established processes and standards Reading, understanding and adhering to organizational Standard Operating Procedures (SOP) Assisting in establishing and enforcing departmental standards Maintain and review clinical programming SOPs and participating in the modification of company SOPs Working with internal staff to resolve issues and exploring new opportunities to add value to organization and departmental processes Helping others to achieve results and performing other duties as assigned Attending and participating in applicable company-sponsored training Education: Bachelors or Masters degree in computer science, life sciences or related field preferred SAS Certified Professional considered a plus What were looking for 3 + years SAS programming experience in pharmaceutical related industry required (1 year with Masters degree) Experience working with CDISC, SQL and Relational Databases preferred Demonstrated programming skills required Working knowledge and solid understanding of database organization and how to extract data in order to generate listings and reports Proven ability in analyzing data and understanding of medical and/or clinical trial terminology is desirable Proven ability in problem solving and ability to work in group setting and independently; ability to adjust to changing priorities Excellent attention to detail and orientation toward meticulous work Strong interpersonal and communication skills, both verbal and written Strong documentation , organizational skills and ability to project and maintain a professional and positive attitude

Responsibilities: Review client case information and determine required medical records and facilities involved. • Initiate medical record requests via fax, email, portals, or telephonic communication in compliance with HIPAA and client-specific protocols. • Regularly follow up with hospitals, clinics, and third-party record retrieval services (e.g., MRO, CIOX) to track the status of requests. • Escalate delays, incomplete records, or denials to appropriate stakeholders and take corrective action. • Update internal tracking systems, logs, and client databases (e.g., Clio, Filevine, Needles) with current status and notes. • Communicate professionally and clearly with providers, clients, and internal teams via email and calls. • Perform quality checks to ensure completeness and accuracy of received records before submission to legal teams. • Maintain turnaround time (TAT) and service level agreements (SLAs) for all assigned cases. • Review and analyze scanned medical records and bills and summarize them as per the guidelines. • Create concise and accurate summaries of patient medical histories, procedures, diagnoses, and treatment plans for internal use and billing purposes. • Maintain organized records of summarized information, ensuring compliance with legal and regulatory standards. Preferred Tools & Platforms Experience (Mandatory): • Clio, Filevine, Litify, or Needles • Record retrieval platforms (CIOX, MRO, ChartSwap, Sharecare) • SharePoint, Dropbox, Google Drive • Nitro, Microsoft word, excel, outlook. Key Skills: Strong understanding of medical terminology. Excellent written communication skills with attention to detail. Proficiency in Microsoft Office Suite and electronic health record (EHR) systems. Preferred Candidate Profile Bachelors degree in life sciences is mandatory (BPT, MPT, BAMS, BHMS, BUMS, and BDS) Should have proficiency in Typing (30 WPM with 97% of accuracy) Should be flexible with 24*7 shift. Freshers can apply. Package: ~ 3.16 LPA for Freshers ~ up to 4.2 LPA for experienced Preferred Candidate Profile: Graduation is mandatory Should be flexible with 24*7 shift. Learning Opportunities Freshers can also apply, must have knowledge about medical terminologies Great work culture Positive Work Environment Immediate Joiners only *** Walk In Details Venue - Provana, A-5 Sector 6 Noida. Time - 10 AM IST Date - 21th June 2025 (SATURDAY) HR Reference : YAMINI MOURYA || PINKI JHA

Greetings From Access Healthcare!! ! Need freshers with Life Science / Para- medical / Ancillary Medical courses Applicable only to candidates with strong knowledge in Human Anatomy and Physiology. Candidates must be prepared on 11 systems in Anatomy and physiology/Medical terminology/abbreviations/patho-physiology - Curriculum Candidates with certification will be preferred most. Work location: Chennai (Ambattur IE) Work mode: Work from office Interview Mode: Face to Face Walk-in Venue : Access Healthcare Headquarters, A9, 1st Main Road, Ambattur Industrial Estate, Chennai - 600058 Interview date and timing: 18, 19, 20 & 21st June 2025, 11 AM onwards Looking for immediate Joiners. Shift: Day Shift All Must Bring Updated Resume With Aadhar Card contact praveen 9655581000 only watsapp praveen.t@accesshealthcare.com

Greetings From Access Healthcare!!! Walk-in drive for Medical coding freshers, Please read below details carefully. Need freshers with Life Science / Para- medical / Ancillary Medical courses Only 2024 & 2025 Passout students are eligible. Applicable only to candidates with strong knowledge in Human Anatomy and Physiology. Candidates must be prepared on 11 systems in Anatomy and physiology/Medical terminology/abbreviations/patho-physiology - Curriculum Candidates with certification will be preferred most. Work location: Chennai (Ambattur IE) Work mode: Work from office Interview Mode: Face to Face Walk-in Venue : Access Healthcare Headquarters, A9, 1st Main Road, Ambattur Industrial Estate, Chennai - 600058 Interview date and timing: 18, 19, 20 & 21st June 2025, 11 AM onwards Looking for immediate Joiners. Shortlisted should join us before 27th Jun 2025 Shift: Day Shift All Must Bring Updated Resume With Aadhar Card

SUMMARY Job Summary: Exciting job opportunity as a Staff Nurse Key Responsibilities: Providing comprehensive patient care, including personal care and medical attention. Adhering to the medical instructions and orders prescribed by doctors. Maintaining accurate and organized patient case records. Administering medications as per doctor's prescriptions. Ensuring patient comfort and safety by repositioning them regularly. Requirements Educational Qualification: Bachelor's Degree in Nursing or GNM Experience: Minimum 6 months working experience as a Nurse Age limit: 18 to 35 years Certification: registration Certification from Nursing Council Language: Basic English proficiency required, Clinical Skills: Bed side nursing, patient care, patient assessment and monitoring Even if you don’t meet all requirements, apply now and let our experts assess your eligibility!

Walk-in drive for Medical coding freshers, Please read below details carefully. Need candidates with Nursing , Pharma & Allied health Science degree Only 2024 & 2025 Passout students are eligible. Candidates must be strong knowledge in Human Anatomy & Physiology. Work Location : Ambattur IE Interview location : Accesshealthcare, HQ , A9 , 1st Main Road, Ambattur IE, Chennai - 600058. Land Mark - Near AIEMA techcentre. Interview Date : 17th to 21st Jun 2025 Interview timing : 11.30 am to 4.00 pm

Preferred candidate profile : Diploma with Minimum 4+ Years experience as Dialysis Technician in Hospital For inquiries, kindly reach out to - Mr. Hament, at 7011324972 or via email at hament.gautam@fortishealthcare.com

Works with a team of Medical regulatory writers with different levels of expertise, Develops medical expertise within Medical regulatory writing (on contents, methods, and processes). Ensures compliance with regulatory requirements from various regions (FDA, EU others) for activities supported. Coordinates and supports medical activities related to the maintenance of the marketing authorizations of Established and Generic products, in different therapeutic areas. Works in close collaboration with Global Medical Leads, Global Regulatory Affairs, Global Pharmacovigilance, and vendors Essential Job duties and responsibilities: Responsible to provide a medical assessment with relevant and updated clinical evidence and monitoring the execution of strategic documents such as PBRERs, ACOs, DSURs, Clinical Overviews, Benefit-Risk assessments, Expert statements for MDD, Responses to Health Authority Queries, Ad-hoc literature analyses, and labeling documents for the corresponding therapeutic area or products or any other activities which are the core activities of GMLs. Drafting the extended synopsis of studies in collaboration with RWE experts. He/she will be responsible for overseeing the execution of such plans by the respective operational units in compliance with SOP, GCP, and other regulations. Writing of Key medical/clinical parts of Common Technical Documents (CTD) or Briefing packages (BP). Reviewing and approving compassionate use of individual medical requests for use of Sanofi medicinal products for serious or life-threatening diseases for treatment outside of clinical trials. Secure delivery of high-quality medical documents on time and in compliance with internal and external standards. Collaborates effectively with stakeholders: global medical leads/ medical product leads, global regulatory affairs, medical regulatory writing global or local teams, pharmacovigilance teams, managed access program teams. People: Maintain effective relationships with the end stakeholders (Medical, regulatory, pharmacovigilance community) within the allocated Global business unit and product with an end objective to develop medical regulatory content as per requirement, 2) Interact effectively with stakeholders in medical and pharmacovigilance departments 3) Constantly assist the medical regulatory writing team in developing knowledge and sharing expertise Performance: Secure deliverables (PBRER, ACO, SO, CSR, ID Cards, Investigator brochure, clinical evaluation report, briefing packages, medical section of CTA, CTD, SBRAs, MDD, HAQs or any other activities which are core activities for GMLs) are supported as per agreed timelines and quality Process: Provide medical strategic insights & evaluation related to Company's portfolio. Contribute to the management of the marketing authorization dossiers of the current related portfolio. Act as an expert in the field of medical regulatory writing and maintain the regulatory requirement for countries, and teams supported. Assist the assigned medical team in conducting comprehensive medical regulatory writing-needs analysis Implement relevant elements of the medical regulatory plan and associated activities for the year identified for the region Work with selected vendors when required within the region to deliver the required deliverables as per the defined process Assist the head of scientific communications in designing an overall plan of action based on end-customers feedback & improving course content and delivery. Stakeholders : Work closely with medical teams in regions/areas to identify medical writing needs and assist in developing assigned deliverables Liaise with the Medical department to ensure relevant & customized are delivered per expectation About you Experience : 5 years of experience supporting international pharmaceutical companies: medical affairs, clinical development, pharmacovigilance with experience in at least one of the therapeutic areas- cardiovascular, metabolism, diabetes and lipid, CNS, oncology, anti-infectives, internal medicine Soft skills : Stakeholder management; communication skills; and ability to work independently and within a team environment Technical skills : As applicable (Including but not limited to Medical operational excellence, time, and risk management skills, Excellent technical (medical) editing and writing skills) Education : Medical degree MBBS; MD Languages : Excellent knowledge of the English language (spoken and written)