Medical Writer - Pharmaceuticals (3-5 Yrs Exp)

We are seeking an experienced Medical Writer with a Diploma in a relevant field and 3-5 years of experience to join our dynamic team. The ideal candidate will be responsible for creating clear, accurate, and scientifically sound medical documents. This role requires a strong understanding of regulatory requirements and the ability to translate complex scientific information into easily understandable content for various audiences.

Key Responsibilities:

Draft, edit, and review various medical documents, including clinical study reports (CSRs), Investigator's Brochures (IBs), protocols, and regulatory submission documents.

Ensure all medical documents are scientifically accurate, clear, concise, and compliant with relevant regulatory guidelines (e.g., ICH, FDA, EMA).

Collaborate with cross-functional teams, including clinical research, regulatory affairs, and R&D, to gather information and ensure alignment on document content.

Manage multiple projects simultaneously, adhering to strict deadlines and maintaining high-quality standards.

Contribute to the development and maintenance of style guides and templates for medical documentation.

Stay updated on the latest advancements in medical writing, pharmaceutical industry trends, and regulatory requirements.