Senior Medical Writer

Healthminds; Bengaluru; Remote; INR 1,500,000 - 2,300,000; Full time

Benefits offered by this job

Medical Insurance

Job summary

HealthMinds Consulting Private Limited is seeking a Medical Writer to develop high quality scientific content for marketing and clinical purposes. You will ensure regulatory compliance, manage references in Veeva Vault PromoMats, and act as a topic expert across several therapy areas.

The role requires 5–10 years in medical writing, PhD/MD or M.Pharm, and mandatory familiarity with MLR processes and promotional asset review.

Qualifications

• PhD/MD or M.Pharm degree required.
• 5–10 years in medical writing or related pharma/life sciences.
• Experience in medical communications.
• Strong understanding of therapy areas and regulatory guidelines.
• Familiarity with MLR processes and Veeva Vault PromoMats is mandatory.
• Knowledge of promotional asset development, referencing and tagging of claims is mandatory.

Responsibilities

• Develop high quality medical communications for marketing and clinical purposes.
• Create submission ready documents; ensure regulatory compliance.
• Review content and provide feedback to meet client needs.
• Ensure adherence to MLR approvals; manage references in Veeva Vault PromoMats.
• Interpret clinical data and conduct literature reviews.
• Collaborate with cross functional teams to meet timelines.
• Provide expertise across multiple therapy areas.

Education

PhD/MD or M.Pharm

Tools

Veeva Vault Promomat

MLR processes

Promotional asset review

Referencing & tagging

Job description

HealthMinds Consulting Private Limited | Full time

CompanyName : HealthMindsConsulting Private Limited

WorkMode : Full-time | Remote

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

• MedicalInsurance
  

Overall Purpose of the Job

The Medical Writer is responsible fordeveloping high-quality scientific and medical content for marketing, and clinicalpurposes. This includes creating submission-ready documents, ensuringcompliance with medical, legal, and regulatory standards, and serving as thesubject matter expert for scientific writing within the team.

Key Responsibilities

• Content Development:
• Create accurate, clear, and compliant medical communicationsfor various channels (e.g., Veeva-approved emails, CLMs, websites,videos).
• Draft and review promotional and educational materials formedical affairs.
• Review content/creative files developed from master assets andprovide feedback based on client requirements
• Regulatory & Compliance:
• Ensure adherence to Medical Legal Regulatory (MLR) approvalprocesses.
• Manage referencing and annotation in Veeva Vault PromoMats.
• Perform reference and annotation of the promotional assets ofVeeva Vault Promomat for further processing.
• Scientific Expertise:
• Interpret and document clinical data accurately.
• Conduct literature searches and analyze client assets forevidence-based content.
• Communicate effectively with cross-functional stakeholders tomeet timelines.
• Provide intellectual input across multiple therapy areas(oncology, respiratory, cardiology, dermatology, vaccines, infectiousdiseases, nephrology, rare diseases).

Qualifications:

• Education: PhD/MD, or M.Pharm.
• Experience:
• 5–10 years in medical writing or related roles in pharma/lifesciences.
• Prior experience in medical communications.
• Skills:
• Strong understanding of therapy areas and regulatoryguidelines.
• 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.