Role & responsibilities

Job Title: Medical Writer

Level: Sr Analyst

Reports To: Senior Manager

Location: India

Overall Purpose of the Job 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, transparent, 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
Education: MBBS, MD, or M.Pharm.
Experience:

o 510 years in medical writing or related roles in pharma/life sciences.

o Prior experience in medical communications and regulatory documentation.
Skills:

o Robust 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.

Preferred candidate profile

📌 Medical Writer Mumbai
🏢 Manpowergroup Services India
📍 Mumbai