10 Clinical Evaluation Jobs

As a Consultant in Internal Medicine, you will be responsible for providing comprehensive care to adult patients with various medical conditions. Your role is crucial in accurately diagnosing conditions, creating effective treatment plans, and managing overall patient care to ensure high-quality healthcare and improved patient outcomes. Collaboration with other healthcare professionals, leading clinical practices, and continuous quality improvement are key aspects of this position. Keeping updated on the latest medical advancements, incorporating evidence-based practices, and maintaining the highest ethical standards are essential. This challenging yet rewarding role requires a combination of in-depth knowledge and a compassionate approach to patient care. Key Responsibilities - Conduct comprehensive evaluations of patients" health status. - Diagnose and develop treatment plans for a wide range of medical conditions. - Provide management of chronic illnesses and preventive care. - Collaborate with specialists to ensure integrated patient care. - Perform necessary diagnostic procedures and interpret results. - Monitor patient progress and adjust treatment plans as necessary. - Educate patients about their conditions and treatment options. - Document patient encounters accurately in electronic medical records. - Participate in clinical audits and quality improvement initiatives. - Mentor and supervise residents and junior medical staff. - Conduct research in relevant areas of interest within internal medicine. - Stay informed about advances in internal medicine and related fields. - Participate in community outreach and health promotion activities. - Ensure compliance with medical regulations and ethical standards. - Provide on-call services for emergency consultations as required. Required Qualifications - MD or DO degree from an accredited medical school. - Board certification in Internal Medicine. - Valid medical license to practice in the relevant state. - A minimum of 5 years of clinical experience in internal medicine. - Strong understanding of general medicine and patient-centered care. - Excellent interpersonal and communication skills. - Ability to work collaboratively within a multidisciplinary team. - Proficient in electronic medical records and healthcare technology. - Commitment to continuous professional development. - Strong analytical and decision-making skills. - Experience in research and clinical trials (preferred). - Ability to manage a diverse patient population. - Strong organizational and time management skills. - Knowledge of healthcare regulations and ethical guidelines. - Demonstrated leadership abilities within a medical setting. - Willingness to participate in community health initiatives.,

The healthcare team in Varanasi is looking for a dedicated and experienced Senior BAMS Physician to join them. As a Senior BAMS Physician, you will be responsible for providing expert Ayurvedic consultation and treatment to patients. Your role will involve diagnosing health issues, prescribing Ayurvedic therapies and medicines, maintaining patient records, and collaborating with other medical professionals for holistic care. Additionally, you will educate patients on Ayurvedic lifestyle practices and ensure high standards of hygiene, safety, and compliance within the clinic or hospital. To qualify for this position, you must have a Bachelor's degree in Ayurvedic Medicine and Surgery (BAMS) from a recognized institution, with a minimum of 5-6 years of clinical experience in a reputed Ayurvedic hospital or clinic. You should have a strong knowledge of Ayurvedic formulations, Panchakarma, and traditional therapies, along with excellent communication and interpersonal skills. The ability to handle a high volume of patients with patience and empathy is essential for this role. Preferred qualifications include experience in handling chronic cases such as arthritis, skin disorders, and digestive issues, as well as certification or experience in Panchakarma therapy. This is a full-time position based on-site in Varanasi, with a day shift schedule. If you meet the requirements and are interested in this opportunity, please send your CV for consideration.,

As a Clinical Evaluation Medical Writer at Medtronic, you will play a crucial role in developing and updating clinical evaluation documents to support CE Mark submissions and ensure compliance throughout the product lifecycle. Your work will involve close collaboration with cross-functional teams to gather and interpret data on device safety, performance, and benefit-risk according to MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745. You will also be responsible for summarizing and disseminating clinical literature and other available data to share relevant evidence, while managing Medical Information activities. This includes tracking inquiries, monitoring key metrics, researching and responding to technical and clinical questions from internal teams and external healthcare professionals under the guidance of Clinical and Medical Affairs. Success in this role will require strong skills in scientific writing, literature review, data analysis, and clear communication, as well as a proactive and collaborative mindset. Your responsibilities may include independently creating and maintaining clinical evaluation documents in compliance with relevant regulations and company procedures, supporting Medical Information activities by responding to inquiries, conducting literature searches and reviews, reviewing scientific materials for accuracy and compliance, developing reports, identifying and reporting complaints or adverse events, and collaborating with key stakeholders to drive evidence-based scientific decisions. To excel in this position, you are required to have a mastery of a specialty area and full knowledge of industry practices, typically obtained through advanced education combined with experience. A Baccalaureate degree and a total of 8 years of experience with a minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years of relevant experience are also required. Medtronic offers a competitive salary and flexible benefits package as part of its commitment to employees. The company values the contributions of its employees and offers various benefits, resources, and competitive compensation plans designed to support you at every career and life stage. The position is also eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). Medtronic is a global leader in healthcare technology that aims to address the most challenging health problems facing humanity by seeking out innovative solutions. With a mission to alleviate pain, restore health, and extend life, Medtronic unites a global team of passionate individuals who are committed to making a difference. The company values diversity and is dedicated to engineering extraordinary solutions for real people by leveraging talent, diverse perspectives, and ambitious ideas. To learn more about Medtronic's business, mission, and commitment to diversity, please visit their website.,

Job Purpose : (what contribution is this position supposed to make in business?) The QMS and EU MDR Compliance Executive is responsible for ensuring compliance with ISO 13485, EU MDR (Regulation EU 2017/745), and other applicable quality and regulatory requirements. This role will support the development, implementation, and maintenance of the Quality Management System (QMS), oversee documentation control, conduct internal audits, and support regulatory submissions and audits as required. Key Deliverables/Responsibilities of this position 1- Quality Management System (QMS): Maintain and improve the ISO 9001:2015 / ISO 13485:2016-compliant Quality Management System. Ensure effective implementation of quality procedures and policies. Manage document control, change control, CAPA, non-conformances, and risk management processes. Coordinate internal audits, supplier audits, and management reviews. Monitor key quality metrics and report quality performance. 2- EU MDR Compliance: Ensure ongoing compliance with EU Medical Device Regulation (EU MDR 2017/745). Support the preparation and maintenance of technical documentation in accordance with Annex II and III of EU MDR. Work with cross-functional teams to ensure products meet General Safety and Performance Requirements (GSPRs). Coordinate with Notified Bodies during audits and technical file reviews. Support UDI, PMS (Post-Market Surveillance), and vigilance processes under EU MDR. 3- Regulatory Affairs: Assist with regulatory submissions and CE marking activities. Maintain up-to-date knowledge of applicable regulatory requirements and changes. Liaise with regulatory consultants, Notified Bodies, and competent authorities as needed. 4- Assist in compilation of technical files & related documentation: • Preclinical studies • Usability engineering as per EN 62366 • Risk management reports – as per 14971 • Clinical evaluation reports – as per MEDDEV 2.7.1 5- Knowledge of EU Regulation (EU) 2017/745, to prepare & compile: • Post Market Clinical Follow up (PMCF) • It is the requirement of EU MDR, Annex XIV • PMCF shall be understood to be a continuous process that updates the clinical evaluation • Post Market Surveillance (PMS) • It is the requirement of EU MDR • Labelling requirements • It Is related to Labeling requirements of medical devices as per EU MDR. Means candidate must understand the related requirements & standard knowledge. • UDI requirement. • It Is also related to Labeling requirements of medical devices as per EU MDR. UDI is the new requirement which must be present in CE certified product labels. • Unique device Identification. 6- Preparation and amendments of quality system procedures 7- Assist in external audits & internal audits 8- Knowledge of Quality Control Operations & Problem Solving & Continuous Improvement Required Technical Skills: Knowledge of ISO 13485 & Regulation (EU) 2017/745 Required Behavioural Attributes: Good learner Interactive with team Good communication skills

You are a qualified and experienced medical professional sought to join the insurance operations team to handle and review Group Personal Accident (GPA) and Group Mediclaim (GMC) claims. Your responsibilities include ensuring the accuracy and appropriateness of claims, resolving medical disputes, addressing client grievances, and providing expert support in claim-related discussions with insurers and clients. Your key responsibilities will involve scrutinizing GPA and GMC claims from a medical perspective, handling disputed or complex claims such as accidental disability or death due to medical or accidental causes, and liaising with insurance company doctors and TPAs to resolve disputes based on clinical merit. Furthermore, you will be responsible for managing medical grievances, addressing customer concerns with medical aspects or claim rejections, and coordinating with corporate clients, insurance company medical teams, TPAs, and legal teams when necessary to ensure clarity and resolution on medical matters. Maintaining detailed and confidential medical case notes for claims handled, documenting recommendations, approvals, and medical assessments, and ensuring alignment with internal policies and industry regulations will also be part of your duties. To excel in this role, you should possess strong clinical evaluation and documentation review skills, a good understanding of insurance terms and claims processes, the ability to assess disability and accidental claims from a medico-legal standpoint, excellent communication and interpersonal skills, and a problem-solving mindset with attention to medical and procedural details. Your qualifications should include an MBBS/BAMS/BHMS degree, with additional qualifications in insurance or healthcare administration being advantageous. You should have at least 3-5 years of experience in medical claims review in the insurance or TPA industry, along with familiarity with claim adjudication processes in Group Health and Personal Accident Insurance.,

Role & responsibilities Design effective product launch & training strategies to improve usage and adoption of UTD and Lexicomp, working clinical departments within hospital and academic institutions • Deliver engaging onsite and Live online (remote) training to end users to increase usage and awareness within each site • Ability to interface with customer contacts at all levels, to develop and strengthen relationships with multiple key contacts and influencers who can support, promote, and coordinate the promotion and use of our products • Uncover and address access challenges and resolve any technical barriers to usage • Provide consistent account feedback and market data to the sales, marketing and product teams. • Maintain accurate account and training activity reports for department month end reporting. • Support the product knowledge enablement of our resellers • Mentor new hires to support their product knowledge • Performs other duties as assigned Preferred candidate profile Strategic Communication: High level of communication skills tailored to various audience needs. • Customer Insight: Deep understanding of customer behavior and needs . • Clinical insights: Clinical point of view from clinician experience. • Advanced Analytical Skills: Ability to deeply analyze performance metrics. Technical Troubleshooting: Proficiency in resolving advanced technical issues. • In-depth Product Knowledge: Comprehensive knowledge of all product features and updates. • Leadership: Ability to provide guidance and mentorship to peers. • Customer Advocacy: Promote customer interests within the organization. • Technical Proficiency: Advanced skills with CRM software and support tools . Requirements: • Fluent in English (written, reading and spoken) local languages would be and strong advantage • Clinical background- with good experience in training/training. • Experienced with remote training and e-learning • Educated - BS/BA Degree or equivalent (medicine/pharmacy/nursing) • Excellent communication and presentation skills • Self-starter, highly organized with ability to prioritize work efficiently and effectively • Strong technical aptitude Excellent Microsoft skills using Word, Excel and PowerPoint, as well as a good understanding of a CRM system (Salesforce.com, SalesLogix or similar) • A team player and able to work independently when needed • Willing and able to travel to customer sites (average 60% travel will vary by quarter) • A valid drivers licens Thank you! Meenakshi Dixit meenakshi_dixit@persolkelly.com www.persolkelly.co.in ------------------------------- CONFIDENTIAL NOTE: By submitting your resume or personal data, you acknowledge reading and agreeing to our Privacy Policy . You hereby provide voluntary consent to the collection, use, processing, and disclosure of your data by us and our affiliates, in line with the Privacy Policy . and applicable laws. If you wish to withdraw your consent or have any concerns, you may submit a request to our designated consent manager, as outlined in our Privacy Policy . We prioritize your privacy. SECURITY NOTE: We at PERSOLKELLY India or our representatives, do not ask job seekers for fees, personal banking information, or payments through unofficial channels. Official communications will only come from @persolkelly.com. Report any suspicious activity to Contactus_in@persolkelly.com . Click here to find out how you can safeguard yourself from job scams. --------------------------------------

We are looking for a skilled and detail-oriented QA Executive to join our team. The candidate will be responsible for ensuring the quality and regulatory compliance of medical devices in line with EU MDR 2017/745 and Indian Medical Device Rules (IMDR). This role involves preparing, reviewing, and updating key technical and regulatory documentation and supporting post-market surveillance activities. Roles & Responsibilities Preparation, review, and updating of Technical Files as per EU MDR 2017/745 and Device Master Files (DMF) as per IMDR . Maintenance of General Safety and Performance Requirements (GSPR) documentation in compliance with applicable guidelines. Preparation of Risk Management Plans and Reports as per ISO 14971 and other applicable standards. Development and review of Clinical Evaluation Protocols and Reports (CEP/CER) as per MDR/IMDR guidelines. Preparation and maintenance of Post-Market Surveillance (PMS) , Post-Market Clinical Follow-up (PMCF) , and Periodic Safety Update Reports (PSUR) . Documentation of Design and Development activities, ensuring alignment with regulatory and internal design control requirements. Drafting and reviewing Usability Engineering Protocols and Reports in compliance with ISO 62366. Monitoring, tracking, trending, and reporting of all reportable events , including serious/adverse incidents and field safety corrective actions (FSCA) . Keeping up to date with current national and international regulations, standards, and best practices relevant to the medical device industry. Ensure proper handover of responsibilities to designated personnel during absence. Desired Candidate Profile Prior experience in quality assurance or regulatory affairs for medical devices. In-depth understanding of EU MDR 2017/745 , IMDR , and related standards (e.g., ISO 13485, ISO 14971, ISO 62366). Strong documentation and review skills. Attention to detail with good organizational and analytical abilities. Effective communication skills and the ability to work independently as well as in a cross-functional team.

Experience & Eligibility Criteria: 2-6 Years of experience with literature searches/ electronic literature databases and Clinical Evaluation Report (CERs) documents writing Education in any UG/PG in Life Science (1st Pref B/M Pharmacy). Job Description: Scientific Analyst (Scientific Literature search) Design of literature searches to be implemented in electronic literature databases Conducting systematic/targeted/structured literature reviews Developing and performing database searches and writing protocols and reports for literature reviews Identifying relevant evidence for research questions (Literature Screening) Summarizing literature review findings in a report Extracting, analyzing, and summarizing data from a range of sources Performing quality checks to ensure data accuracy Providing writing support for Clinical Evaluation Report (CERs) documents Communicating with the internal project team to ensure smooth and timely execution of the projects.

Roles & Responsibilities Ensure on-time development and delivery of various sections of high-quality regulatory documents compliant with MEDDEV 2.7/1 Rev. 4. and MDR for Medical Devices across therapeutic areas Actively engage with internal stakeholders and cross-functional client business teams such as Medical Directors, Post Market Surveillance, Design Quality Engineers, R&D, and Regulatory Affairs Deliver solutions that are customized per client requirements in terms of language, content, format, and presentation Assist the Team Lead/Manager in the development of schedules to ensure timely delivery Manage timelines and communicate with team members to maintain awareness of expectations, milestones, and deliverables Train and mentor junior members of the team on technical/process related aspects Conduct proofreading, editing, document formatting, review comment incorporation and document completion / approval activities Perform literature searches on various databases Screening, appraisal per pre-defined criteria, and summarization of articles Interpret and present data from device-specific technical documents such as User Manuals/Instructions for Use Summarize quantitative data from post-marketing surveillance Conduct editing, proofreading, document formatting, and other document completion/approval activities Education Bachelors Degree / Post Graduation in any relevant Life Sciences field. Masters Degree is preferred. Experience Publication experience in scientific journals preferable Minimum 3 years of experience in Medical Device Regulatory documentation Familiarity with the Life Sciences Industry, preferably Regulatory Services Hands on experience on CEP/CER/PMSR/PSUR process Experience in creating high quality deliverables for customers Experience in handling projects and engaging with multiple clients independently Experience of working on projects involving all devices classes from various Therapeutic Areas Technical/Functional Skills Knowledge of clinical evaluation and related documents and regulatory requirements Proficiency in comprehension of scientific data and medical terminology and efficiency in summarizing information from source documents and published literature Proficiency with Microsoft Office (Word, Excel, and Outlook) Hands on experience on presentation tools such as PowerPoint, Visio etc., and referencing tools such as Zotero, Endnote, etc. will be an added advantage Effective reviewing skills for review of work done by trainees/junior writers Non-Technical Skills Strong verbal and written communications skills Ability to work as part of a team A constant zeal towards learning and skill development Potential to multitask and work within timelines Ability to understand and deliver on customer requirements Mentoring skills to act as trainer/mentor for junior members of the team Personal Traits Positive Attitude Initiative and Commitment Detail Oriented Team player Focused and sincere Perseverance Competencies Basic English grammar, punctuation, and sentence construction Logical comprehension Knowledge of medical terminology Excellent Communication (Writing and Verbal) Quality focused mindset Good time management Good stakeholder management

Experienced and licensed medical professional (MBBS/MD) with a strong background in medical claims assessment and clinical evaluation within the health insurance or TPA industry. Skilled in reviewing pre-authorization requests, hospitalization claims, and medical documentation to ensure medical necessity, policy compliance, and regulatory standards (IRDAI). Proficient in ICD-10 coding, claims adjudication, and fraud detection, with a focus on accuracy, ethical judgment, and collaborative decision-making. Adept at coordinating with hospitals, TPAs, and internal teams to streamline claim processing and maintain service quality.