Job Description
Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a New
Dimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research,
Medical/Scientific Support and Emerging Region Expansion
Job description: Senior Medical Writer
Writing and reviewing clinical/regulatory documents such as clinical trial protocols, clinical study reports/Clinical evaluation reports, investigator brochures, informed consent forms, and according to ICH or other guidelines.
CSR (Clinical Study) or CER (Clinical Evaluation) Module Drafting & Documentation writing.
Publication manuscripts, abstracts, posters (content writing) and presentations participate in post-market surveillance activities by conducting routine systematic literature reviews (e.g. Screening of articles against inclusion/exclusion criteria, extracting data from included studies,
Interpreting study results and preparing summaries into formal reports) for specific medical device groups or subgroups.
Develop templates for reports and other regulatory documents.
Education & Qualifications:
Any Bachelor / Masters in Life Sciences Onl
Required: a Minimum of 3-8 years of experience in Medical Writing (CER) or a related field.
We looking for those who join immediately
Qualification
Experience 3- 8
Job Category Medical Writer
Posted On 10/23/2026
Expires On 11/23/2026
💡 Quick Summary
Seeking a career-building opportunity? The Senior Medical Writer position is now open for candidates interested in the Content Writer Jobs sector. This role in Hyderabad offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Content Writer Jobs is a plus.
