Are you an experienced Medical Writing professional in the medical device industry looking for an opportunity in Bengaluru? ClinChoice is hiring a Scientist – Medical Writing (Shared Services) to support Clinical Evaluation Reports (CER) and Safety Surveillance Reports (SSR) for global medical device businesses.
This Medical Writing job in Bengaluru is ideal for candidates with strong expertise in clinical evaluation report writing, regulatory compliance, CER documentation, and safety surveillance processes within the medical device domain.
About ClinChoice
ClinChoice is a global clinical research organization established in 1995. The company partners with pharmaceutical, medical device, and consumer healthcare innovators worldwide. With delivery centers across the United States, United Kingdom, Japan, China, India, and more, ClinChoice provides expertise in:
- Clinical Operations
- Biometrics
- Regulatory Affairs
- Pharmacovigilance
- Medical Affairs
- Toxicology
The organization is known for accelerating clinical trials, supporting regulatory compliance, and strengthening patient safety systems globally.
Job Title
Scientist – Medical Writing (Shared Services)
Location: Bengaluru, Karnataka
Industry: Medical Devices / Clinical Research / Regulatory Affairs
Key Responsibilities – Medical Writing (CER & SSR)
The Scientist – Medical Writing will focus on Clinical Evaluation Report (CER) and Safety Surveillance Report (SSR) processes within the medical device business.
Core Responsibilities:
- Writing and maintaining Clinical Evaluation Plans (CEPs)
- Compliant authoring of Clinical Evaluation Reports (CERs) as per regulatory and client guidelines
- Preparation of Safety Surveillance Reports (SSRs)
- Ensuring CER/SSR documentation aligns with:
- Risk Management files
- Post Market Surveillance (PMS)
- Quality Systems documentation
- Partnering with cross-functional teams including:
- Medical Directors
- Regulatory Affairs
- Post Market Surveillance
- Design Quality Engineering
- R&D teams
- Supporting regulatory audits and Notified Body inspections
- Monitoring global regulatory trends related to CER requirements
- Ensuring timeline adherence for CER/SSR deliverables
This role requires in-depth understanding of medical device regulatory writing and clinical evidence generation.
Qualifications & Eligibility Criteria
Educational Qualification:
- Graduate or Post-graduate in Life Sciences
Experience:
- Minimum 3 years of experience in:
- Medical Writing
- Technical Writing
- Scientific Writing
Mandatory Experience:
- Experience in the medical device industry
- Strong knowledge of:
- Clinical Evaluation Reports (CER)
- CER regulatory requirements
- Evidence generation
- CER document preparation
Preferred Skills:
- Knowledge of:
- Quality regulatory compliance
- Complaint handling
- Adverse event reporting
- Medical device risk management
- Biostatistical methods
- Regulatory/Notified Body audit exposure
Salary & Career Growth
For a Scientist – Medical Writing role in Bengaluru within the medical device sector, the estimated salary range is:
₹9,00,000 – ₹14,00,000 per annum (CTC)
(Based on experience and domain expertise)
Working with ClinChoice offers:
- Exposure to global regulatory frameworks
- Cross-functional collaboration with international stakeholders
- Growth in medical device regulatory writing
- Involvement in global audits and inspections
- Strong career pathway in Clinical Evaluation & Regulatory Affairs
Why This Medical Writing Job Is Important
With evolving EU MDR and global regulatory frameworks, Clinical Evaluation Reports (CER) and Safety Surveillance Reports (SSR) are critical to maintaining market access for medical devices. This Scientist – Medical Writing role plays a key part in ensuring regulatory compliance and patient safety.
For professionals aiming to build expertise in medical device regulatory medical writing, this position offers strong long-term career value.
How to Apply
