The Medical Writer is responsible for developing high-quality scientific and medical content for marketing, clinical, and regulatory purposes. This includes creating submission-ready documents, ensuring compliance with medical, legal, and regulatory standards, and serving as the subject matter expert for scientific writing within the team.
Key Responsibilities
• Content Development:
o Create accurate, explicit, and compliant medical communications for various channels (e.g., Veeva-approved emails, CLMs, websites, videos).
o Draft and review promotional and educational materials for medical affairs.
• Regulatory & Compliance:
o Ensure adherence to Medical Legal Regulatory (MLR) approval processes.
o Manage referencing and annotation in Veeva Vault PromoMats.
• Scientific Expertise:
o Interpret and document clinical data accurately.
o Conduct literature searches and analyze client assets for evidence-based content.
• Collaboration:
o Communicate effectively with cross-functional stakeholders to meet timelines.
o Provide intellectual input across multiple therapy areas (oncology, respiratory, cardiology, dermatology, vaccines, infectious diseases, nephrology, rare diseases).
Qualifications
• Experience:
o 5–10 years in medical writing or related roles in pharma/life sciences.
o Prior experience in medical communications and regulatory documentation.
• Skills:
o Solid understanding of therapy areas and regulatory guidelines.
o Excellent writing, editing, and communication skills.
o Familiarity with Veeva systems and MLR processes
Preferred Attributes
• Ability to work independently and manage multiple projects.
• Strategic thinking and creativity in content development.
• Robust problem-solving and critical thinking skills.
📌 Senior Medical Writer Mumbai
🏢 Trigent Software
📍 Mumbai
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