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Chief Manager – Medical Writer

3-5 years
Not Disclosed
10 April 11, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Chief Manager – Medical Writer

Location: Mumbai, Maharashtra, India (Kurla)
Department: Regulatory Affairs
Business Unit: Piramal Critical Care (PCC)
Travel Requirement: Low
Reporting To: Vice President, Regulatory Affairs
Job ID: Not specified


Job Overview

Responsible for creating scientifically accurate and regulatory-compliant documents to support drug development, regulatory submissions, and medical communications. This role involves interpreting complex clinical data and translating it into clear content for various stakeholders including regulatory authorities, healthcare professionals, and internal teams.


Key Stakeholders

  • Internal: IT, Regulatory Affairs, Pharmacovigilance, Medical Information

  • External: Healthcare Professionals, Publications, IT Developers, Health Authorities


Essential Qualifications

  • Master’s or PhD in Life Sciences, Pharmacy (M.Pharm, B.Pharm), or Medicine (MBBS, BDS, MD)

  • MBBS or MD preferred

  • Certifications in medical writing (e.g., EMWA, AMWA, ISMPP) are a plus


Experience

  • 3–5 years of experience in the pharmaceutical industry

  • Experience in regulatory affairs, medical affairs, or CROs

  • Familiarity with ICH, FDA, EMA, CDSCO guidelines

  • Experience in writing Company Core Data Sheets (CCDS)


Key Responsibilities

Regulatory Writing

  • Develop and review clinical study reports (CSRs), investigator brochures (IBs), CTDs, protocols, ICFs, and regulatory dossiers.

Scientific & Medical Writing

  • Create high-quality manuscripts, abstracts, white papers, literature reviews, and slide decks for publication or education.

Medical Communications

  • Develop product monographs, training materials, and KOL presentations for internal and external use.

Data Interpretation & Literature Review

  • Perform detailed reviews and analyze clinical/non-clinical data for drug development and post-marketing.

Compliance & Quality Assurance

  • Ensure alignment with global regulatory requirements (ICH-GCP, FDA, EMA, etc.) while maintaining accuracy and clarity.

Cross-functional Collaboration

  • Collaborate with teams including regulatory, clinical research, PV, and medical affairs for document development.


Competencies & Skills

  • Proficient in regulatory and clinical medical writing

  • Knowledge of drug development and clinical trial processes

  • Familiarity with referencing tools (EndNote, Mendeley)

  • Understanding of regulatory submission formats (eCTD, FDA, EMA)

  • Strong research, analytical, and communication skills

  • Proficient in Microsoft Office Suite (Word, PowerPoint, Excel)


About the Company

Piramal Critical Care (PCC), under Piramal Pharma Limited, is a global leader in hospital generics and one of the top producers of inhaled anaesthetics. With a presence in over 100 countries, PCC operates cutting-edge manufacturing units in India and the USA and focuses on sustainable, ethical, and inclusive growth.


Equal Opportunity Statement

Piramal Group is an equal opportunity employer. Employment decisions are based on qualifications, skills, and performance without regard to race, gender, religion, disability, or other protected characteristics.