Instagram
youtube
Facebook

Safety Writer

0-2 years
Not Disclosed
10 April 10, 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: Safety Writer
Location: Mumbai
Category: Clinical
Job ID: 251686


Job Overview:

Responsible for preparing and reviewing safety, risk management, and signal detection documents. Manages safety report deliverables, leads client communications, supports junior writers, and ensures the timely delivery of high-quality documents aligned with regulatory expectations.


Summary of Responsibilities:

  • Lead planning activities, data collection, kick-off meetings, and roundtable comment resolution discussions.

  • Write or co-author global regulatory safety reports: Annual Reports (IND and others), PSURs, PADERs, DSURs, RMPs.

  • Perform quality reviews of safety reports authored by peers or junior writers.

  • Contribute to ad hoc reports, benefit-risk evaluation reports, and labeling support documents.

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

  • Prepare medical information responses for healthcare professionals.

  • Author/contribute to signal reports (periodic/ad hoc) and safety issue analysis reports.

  • Write narratives for adverse drug reactions and serious adverse events.

  • Communicate with internal teams and external clients to gather necessary report inputs.

  • Create and revise labeling documents: Core Data Sheets, USPI, SPCs, Med Guides.

  • Conduct and review literature searches for reports and surveillance; suggest updates to search strategies.

  • Write literature abstracts/summaries and propose company comments.

  • Promote consistency, quality, and efficiency in safety writing processes.

  • Ensure compliance with regulatory requirements and SOPs.

  • Maintain a high standard of customer service and accountability.

  • Perform additional tasks as required by project or manager, post training.


Qualifications (Minimum Required):

  • Bachelor’s degree in life sciences or a related field (or equivalent experience).

  • Demonstrated writing experience in clinical/safety domains.

  • Strong command of written English and scientific communication.

  • Familiarity with regulatory safety writing practices and pharmacovigilance guidelines.


Preferred Qualifications:

  • Advanced degree (e.g., Master’s or PhD) in life sciences or pharmacy.

  • Experience with CTD documentation and global safety reporting standards.


Work Environment:

  • Office-based or remote setting depending on project requirements.

  • Collaborative, client-focused work culture with performance accountability.