As an Associate Medical Writer, you will play a key role in developing clinical documents, collaborating with study groups, and supporting medical affairs activities. This position offers an opportunity to drive cross-functional collaboration, conduct real-world studies, and contribute to global publications.
Key Responsibilities
- Clinical Documentation: Develop study protocols, non-interventional study reports, and investigator brochures following SOPs, timelines, and regulatory guidelines.
- Stakeholder Collaboration: Facilitate document review meetings, coordinate version approvals, and ensure audit-preparedness.
- Research & Publications: Perform literature searches and prepare summaries, abstracts, posters, and presentations for congresses.
- Process Improvement: Share knowledge, implement best practices, and drive process improvements within global teams.
- Medical Affairs Activities: Participate in internal/external events such as expert meetings and conferences.
Qualifications
- Education:
- Degree in life sciences, medical, or pharmaceutical fields.
- Experience:
- 2+ years in medical writing, focusing on study protocols, non-interventional study reports, and investigator brochures.
- Skills & Knowledge:
- Familiarity with diabetes, obesity, and MASH therapy areas.
- Strong literature search capabilities.
- Experience developing abstracts, congress posters, and presentations.
- Good understanding of regulatory guidelines and audit processes.
- Excellent communication and teamwork skills.
- Prior experience in the pharmaceutical or healthcare industry.
