Medical Writer

Manpowergroup Services India; Mumbai; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Manpowergroup Services India is seeking a Senior Medical Writer to develop high-quality scientific and medical content for marketing, clinical, and regulatory purposes. You will create submission-ready documents, ensure compliance with medical, legal, and regulatory standards, and serve as the subject matter expert for scientific writing within the team.

The role requires strong writing and editing skills, familiarity with Veeva systems and MLR processes, and the ability to work with

Qualifications

• MBBS, MD or M.Pharm qualification.
• 5–10 years in medical writing or related pharma/life sciences.
• Experience in medical communications and regulatory documentation.
• Strong writing, editing and communication skills.
• Familiarity with Veeva systems and MLR processes.
• Knowledge of therapy areas and regulatory guidelines.

Responsibilities

• Create accurate, compliant medical communications for various channels.
• Draft and review promotional and educational materials for medical affairs.
• Ensure adherence to MLR approval processes and manage referencing in Veeva Vault PromoMats.
• Interpret clinical data and conduct literature searches to support content.

Skills

Medical writing

Regulatory writing

Editing

Communication skills

Veeva systems

Cross-functional collaboration

Education

MBBS/MD/M.Pharm.

Tools

Veeva Vault PromoMats

Job description

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:
  • Create accurate, clear, and compliant medical communications for various channels (e.g., Veeva-approved emails, CLMs, websites, videos).
  • Draft and review promotional and educational materials for medical affairs.
• Regulatory & Compliance:
  • Ensure adherence to Medical Legal Regulatory (MLR) approval processes.
  • Manage referencing and annotation in Veeva Vault PromoMats.
• Scientific Expertise:
  • Interpret and document clinical data accurately.
  • Conduct literature searches and analyze client assets for evidence-based content.
• Collaboration:
  • Communicate effectively with cross-functional stakeholders to meet timelines.
  • 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:
  • 510 years in medical writing or related roles in pharma/life sciences.
  • Prior experience in medical communications and regulatory documentation.
• Skills:
  • Strong understanding of therapy areas and regulatory guidelines.
  • Excellent writing, editing, and communication skills.
  • Familiarity with Veeva systems and MLR processes

Preferred Attributes

• Ability to work independently and manage multiple projects.
• Strategic thinking and creativity in content development.
• Strong problem-solving and critical thinking skills.

Preferred candidate profile