Senior Medical Writer

HealthMinds Consulting Pvt. Ltd; Bengaluru; Hybrid; INR 1,500,000 - 2,300,000; Full time

Benefits offered by this job

Medical Insurance

Job summary

HealthMinds Consulting Private Limited in Bengaluru seeks a Medical Writer to develop high-quality scientific and medical content for marketing and clinical purposes, ensuring compliance with regulatory standards. You will handle submission-ready documents and serve as SME within the team.

The role requires 5–10 years of pharma/life sciences writing experience, deep therapy-area knowledge, and hands-on experience with Veeva Vault Promomat and MLR processes.

Qualifications

• Advanced medical writing and editing capabilities
• Strong regulatory knowledge and adherence to MLR guidelines
• Experience with Veeva Vault PromoMats and referencing/ tagging claims
• Familiarity with therapy areas including oncology, respiratory, cardiology, dermatology, vaccines, infectious diseases, nephrology, rare diseases

Responsibilities

• Content Development: create accurate, compliant medical communications for multiple channels.
• Regulatory & Compliance: ensure adherence to MLR approval processes and manage annotations in Veeva Vault PromoMats.
• Scientific Expertise: interpret clinical data, conduct literature searches, support evidence-based content.
• Cross-functional communication: work with teammates to meet timelines.

Skills

Medical writing

Regulatory knowledge

Editorial skills

Veeva Vault Promomat

MLR processes

Literature review

Cross-functional collaboration

Education

PhD/MD or M.Pharm

Tools

Veeva Vault PromoMats

Job description

Company Name: HealthMinds Consulting Private Limited

Work Mode: Full-time, On-site & Remote (depending on the project)

Shift: US (5:30 pm to 3 am IST)

• Medical Insurance

Overall Purpose of the Job

The Medical Writer is responsible for developing high-quality scientific and medical content for marketing, and clinical 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.
• Review content/creative files developed from master assets and provide feedback based on client requirements
• Regulatory & Compliance:
• Ensure adherence to Medical Legal Regulatory (MLR) approval processes.
• Manage referencing and annotation in Veeva Vault PromoMats.
• Perform reference and annotation of the promotional assets of Veeva Vault Promomat for further processing.
• Scientific Expertise:
• Interpret and document clinical data accurately.
• Conduct literature searches and analyze client assets for evidence-based content.
• 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: PhD/MD, or M.Pharm.
• Experience:
• 5–10 years in medical writing or related roles in pharma/life sciences.
• Prior experience in medical communications.
• Skills:
• Strong understanding of therapy areas and regulatory guidelines.
• Excellent writing, editing, and communication skills.
• Familiarity with Veeva Vault Promomat and MLR processes (mandatory).
• Knowledge of promotional asset development and review (mandatory).Knowledge of referencing and tagging of claims (mandatory).

Preferred Attributes:

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