Job Title: Senior Safety Writer and Process Lead
Location: Mumbai, India
Job Type: Full-Time
Job ID: 256223
Posted: 30+ Days Ago
Job Category: Pharmacovigilance / Medical Writing / Drug Safety / Regulatory Affairs
Job Overview
We are seeking a highly experienced Senior Safety Writer and Process Lead to oversee the preparation, review, and lifecycle management of aggregate safety reports, risk management documentation, signal detection analyses, and benefit-risk evaluation reports for global regulatory submissions.
This leadership role involves end-to-end responsibility for report planning, authoring, review coordination, approval workflows, and submission readiness. The selected candidate will also act as a process lead, coordinating report writing activities across teams, ensuring regulatory compliance, maintaining quality metrics, and mentoring medical writers within pharmacovigilance operations.
Experience Required
5–7 years of experience in the pharmaceutical industry
Minimum 4+ years of experience in medical writing or safety writing
Experience in pharmacovigilance and drug safety reporting
Experience in drug discovery and clinical safety preferred
Key Responsibilities
Lead preparation and review of aggregate safety reports for global regulatory submissions, including:
Annual Reports (IND and related reports)
Periodic Safety Update Reports (PSURs) / Periodic Benefit-Risk Evaluation Reports (PBRERs)
Periodic Adverse Drug Experience Reports (PADERs)
Development Safety Update Reports (DSURs)
Bridging reports and ad hoc safety reports
Author and review Risk Management Plans (RMPs), Safety Update Reports, Addendum reports, and supporting regulatory documentation
Draft Common Technical Document (CTD) sections including Clinical Overviews, Clinical Summaries, and Non-Clinical Summaries
Generate line listings, summary tabulations, CFIs, and CFCs
Conduct comprehensive literature searches to support report writing and label updates
Create and update labeling documents such as Core Data Sheets (CDS), USPI, centralized SPCs, and Medication Guides
Recommend label changes and prepare justification documentation
Coordinate writing activities across teams, including scheduling, resource allocation, and cross-functional communication
Act as primary client contact for safety report writing activities
Track project metrics, conduct quality checks, and ensure timely deliverables
Mentor medical writers and act as a writing coach
Assist in resource estimation and RFP responses
Ensure compliance with global regulatory requirements, Good Pharmacovigilance Practices (GVP), and ICH GCP guidelines
Promote standardized, efficient, and high-quality processes within safety operations
Required Qualifications
Bachelor’s degree in Life Sciences or related discipline (or equivalent experience)
Strong understanding of pharmacovigilance regulations and global safety reporting requirements
In-depth knowledge of benefit-risk assessment methodologies
Strong understanding of anatomy, physiology, disease states, and medical treatments
Excellent written and spoken English
Strong organizational, analytical, and time management skills
Proficiency in MS Office tools
Strong interpersonal and stakeholder management skills
Preferred Qualifications
Advanced degree (Master’s or PhD) in Life Sciences or related field
Scientific or clinical research background
Experience managing multi-project safety documentation across global teams
Work Environment
Based in Mumbai, India
Work location may include client office assignments and/or home-based setup
Travel requirement: Up to 10%, including occasional overnight travel based on project needs
Why Apply?
This is a senior leadership opportunity for experienced safety writers seeking to advance into a process-focused role within global pharmacovigilance operations. The position offers exposure to international regulatory submissions, cross-functional leadership, and strategic safety documentation management within pharmaceutical and CRO environments.
Gujarat :
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Siliguri |Illinois :
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Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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Kyiv |Lima Region :
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