Role Summary A Clinical Evaluation Manager (often specializing in medical devices) leads the process of collecting, analyzing, and documenting clinical data to demonstrate a device’s safety and performance for regulatory compliance (e.g., EU MDR/MEDDEV 2.7/1 Rev 4). This role acts as a subject matter expert, overseeing medical writers, managing Clinical Evaluation Reports (CERs), and providing strategic input on clinical data requirements throughout the product lifecycle.

Key Responsibilities

- Clinical Evaluation Strategy &
- Documentation:

Develop, maintain, and update Clinical Evaluation Plans (CEPs), Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-up (PMCF) plans, and Summary of Safety and Clinical Performance (SSCP).

- Regulatory Compliance &

- Submissions:

Ensure all documentation adheres to regulatory standards (e.g., MDR 2017/745, MEDDEV 2.7/1 Rev 4) and lead responses to notified body questions.

- Literature Reviews &

- Data Analysis:

Conduct systematic, evidence-based literature searches to obtain clinical data, interpreting complex clinical and risk data to assess the benefit-risk profile of devices.

- Team Leadership &

- Oversight:

Supervise or guide medical writers in the creation of CERs, setting project timelines and ensuring high-quality, timely deliverables.

- Cross-functional Collaboration:

Partner with R&D;, Regulatory Affairs,



Quality Engineering, and Marketing to ensure alignment on product safety and performance, acting as a core team member for recent product development.

- Risk Management Support:

Contribute to risk assessment activities, including updating risk analysis based on clinical data.

Required Qualifications &

- Skills

- Education:

Bachelor’s or Master’s degree in Life Sciences (e.g., Biomedical Engineering, Nursing, Medicine, Pharmacy).

- Experience:

2–5+ years in medical writing, clinical research, or regulatory affairs within the medical device industry.

- Regulatory Knowledge:

In-depth understanding of EU MDR (2017/745), MEDDEV 2.7/1, and ISO standards (ISO 14971, ISO 14155).

- Technical Writing:

Proven ability to produce, review, and edit scientific, clinical, and regulatory documents.

- Analytical Skills:

Strong ability to interpret complex clinical data and peer-reviewed literature.

- Project Management:

Demonstrated ability to manage projects, meet deadlines, and work with cross-functional teams.

Preferred Qualifications

- Advanced Degree:

PhD, MD, or PharmD.

- Certification:

RAC (Regulatory Affairs Certification) or PMP (Project Management Professional).

- Specific Device Knowledge:

Experience in specialized fields (e.g., Cardiovascular/Structural Heart).

📌 Manager Clinical Affairs (Ahmedabad)
🏢 Zydus Group
📍 Ahmedabad