Position Overview
- Join team as an experienced Freelance Medical Writer on a 1-year remote contract.
- Key role in preparing high-quality regulatory and clinical documentation.
- Focus on writing Clinical Study Reports (CSRs), Investigator’s Brochures (IBs), and study protocols.
Job Responsibilities
- Draft and review CSRs, IBs, and study protocols in line with regulatory standards.
- Collaborate with cross-functional teams, including clinical research, regulatory affairs, and biostatistics, to ensure accurate documentation.
- Ensure all documents are clear, concise, and scientifically accurate.
- Stay updated on regulatory guidelines and industry standards.
- Handle multiple projects and meet tight deadlines.
Qualifications
- Bachelor’s degree in Life Sciences, Medicine, or a related field (Advanced degree preferred).
- 10 years of proven experience as a Medical Writer, focusing on regulatory and clinical documents.
- Strong knowledge of regulatory guidelines and clinical research processes.
- Excellent writing, editing, and communication skills.
- Ability to work independently and manage time effectively in a remote setting.
- Proficiency in document management systems and Microsoft Office Suite.
If you are detail-oriented and passionate about contributing to clinical research through expert writing, apply today!
