Medical Writer – Future Roles

This is a fully remote position, open to applicants in India.

📋 Description

• Oversees the precise and thorough execution of medical writing deliverables.

• Manages the medical writing tasks related to specific studies.

• Produces a range of documents such as clinical study protocols, clinical study reports, informed consent forms, and others.

• Complies with established regulatory standards.

• Organizes quality and editorial reviews.

• Serves as a peer reviewer for the internal team.

• Offers technical support, training, and consultation.

⛳️ Requirements

• 3-5 years of pertinent experience in scientific, technical, or medical writing.

• Background in the biopharmaceutical, medical device, or contract research organization sectors.

• Strong comprehension of FDA and ICH regulations, other regulatory guidelines, and/or good publication practices.

• Proven experience in drafting relevant document types.

• Comprehensive knowledge of English grammar and the ability to communicate effectively.

• Well-versed in the AMA Manual of Style.

🏝️ Benefits

• Health insurance.

• Opportunities for career development and advancement.

• Supportive and engaged line management.

• Technical and therapeutic area training.

• Peer recognition.

• Total rewards program.