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Senior Safety Writer

4+ years
Not Disclosed
10 April 10, 2025
Job Description
Job Type: Full Time Education: PhD or Masters 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: Senior Safety Writer
Location: Mumbai
Category: Clinical
Job ID: 251685


Job Overview:

Lead preparation and review of safety-related regulatory documents, manage full report life cycle (planning, authoring, review, approval, and submission), and ensure timely, high-quality deliverables. Guide and mentor junior team members, support project management, and maintain strong client relationships.


Summary of Responsibilities:

  • Author and review safety reports: Annual Reports, PSURs, PADERs, PBRERs, DSURs, ACOs, Addendums.

  • Draft and review RMPs, benefit-risk reports, medical device reports.

  • Write CTD Summaries (Non-Clinical, Clinical Overviews, Summaries).

  • Train and mentor junior writers; provide hands-on learning and coaching.

  • Draft health authority response documents in collaboration with cross-functional teams.

  • Write scientific publications: manuscripts, abstracts, posters.

  • Support medical information queries and author responses.

  • Perform and review signal detection tasks, strategy development, and evaluations.

  • Author/review ad hoc signal reports and safety issue analyses.

  • Develop SOPs, WIs, and other process documentation.

  • Coordinate report writing activities across teams if applicable.

  • Conduct tracking, quality checks, and training activities.

  • Assist in RFP responses and resource estimations.

  • Manage client communications and issue resolution.

  • Prepare and revise labeling documents (CDS, USPI, SPCs, Med Guides).

  • Conduct literature reviews for report authoring and surveillance.

  • Promote quality and compliance across all documentation.

  • Perform additional tasks as assigned.


Qualifications (Minimum Required):

  • Bachelor's degree in Life Sciences (or equivalent).

  • 4+ years in the pharmaceutical industry, with at least 3 years in medical writing.

  • Excellent command of English (written and spoken).

  • Strong MS Office, communication, and organizational skills.

  • Familiarity with regulatory requirements, PV practices, and ICH GCP guidelines.


Preferred Qualifications:

  • Advanced degree (e.g., Master's or PhD).

  • Scientific or clinical research experience.


Work Environment:

  • Office or remote setup.

  • Up to 10% travel, including overnight stays, as per project needs.