Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Safety Writer

Fortrea
3+ years
Not Disclosed
Mumbai, India
1 June 8, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology

Safety Writer

Location: Mumbai
Employment Type: Full-Time
Application Deadline: June 11, 2026
Job Requisition ID: 262799


Job Summary

The Safety Writer is responsible for authoring, reviewing, and managing aggregate safety reports, risk management documents, signal detection reports, and other pharmacovigilance-related regulatory documents. The role involves collaborating with internal teams and clients to ensure the timely delivery of high-quality safety documentation that meets global regulatory requirements.

The Safety Writer also provides quality oversight for junior writers, conducts scientific literature reviews, contributes to benefit-risk evaluations, and supports safety surveillance activities across the product lifecycle.


Key Responsibilities

Safety & Regulatory Writing

  • Author and review aggregate safety reports for global regulatory submissions, including:

    • Annual Reports (IND and Non-IND)

    • Periodic Safety Update Reports (PSURs/PBRERs)

    • Periodic Adverse Drug Experience Reports (PADERs)

    • Development Safety Update Reports (DSURs)

    • Risk Management Plans (RMPs)

    • Other safety-related regulatory documents

  • Take ownership of assigned deliverables and coordinate with stakeholders to obtain required inputs.

  • Ensure documents are completed according to timelines, quality standards, and regulatory requirements.


Safety Surveillance & Signal Management

  • Author and contribute to:

    • Signal Detection Reports

    • Signal Evaluation Reports

    • Safety Issue Analysis Reports

    • Benefit-Risk Evaluation Reports

  • Support ongoing safety surveillance activities.

  • Assist in identifying and evaluating emerging safety signals.


Clinical & Regulatory Documentation

  • Write or contribute to:

    • Common Technical Document (CTD) Summaries

    • Clinical Overviews

    • Clinical Summaries

    • Non-Clinical Overviews

    • Label Update Justification Documents

    • Supporting Regulatory Documents

  • Prepare subject narratives for:

    • Adverse Drug Reactions (ADRs)

    • Serious Adverse Events (SAEs)


Labeling & Risk Management Support

  • Participate in development and maintenance of:

    • Core Data Sheets (CDS)

    • United States Prescribing Information (USPI)

    • Summary of Product Characteristics (SPC)

    • Medication Guides (Med Guides)

  • Support label update activities and associated documentation.


Medical Information & Scientific Communication

  • Prepare medical information responses for Healthcare Professionals (HCPs).

  • Communicate effectively with clients and internal stakeholders to gather and clarify data requirements.

  • Participate in kick-off meetings, strategy discussions, and comment resolution meetings.


Literature Review & Research

  • Conduct scientific literature searches for:

    • Safety Reports

    • Signal Evaluations

    • Routine Surveillance Activities

  • Review and optimize literature search strategies.

  • Evaluate scientific publications for relevance and quality.

  • Author literature summaries, abstracts, and company commentaries.

  • Review literature outputs prepared by junior writers.


Quality Review & Mentorship

  • Perform quality reviews of safety documents prepared by junior and associate medical writers.

  • Ensure consistency, scientific accuracy, and compliance with regulatory standards.

  • Provide guidance and support to less experienced team members.


Compliance & Process Excellence

  • Ensure compliance with:

    • Global Regulatory Requirements

    • Good Pharmacovigilance Practices (GVP)

    • ICH-GCP Guidelines

    • Internal SOPs

  • Promote efficient and high-quality writing processes.

  • Support continuous improvement initiatives.

  • Maintain a strong customer-focused approach while delivering project objectives.


Required Qualifications

Educational Requirements

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Medical Sciences

    • Nursing

    • Related Healthcare or Scientific Discipline

Equivalent relevant experience may be considered in lieu of educational qualifications.


Preferred Qualifications

  • Master's Degree in Life Sciences, Pharmacy, Biotechnology, Medical Sciences, or related field.

  • PhD in a scientific discipline is highly desirable.


Required Experience

Experience Level

  • Minimum 3 years of experience in the Pharmaceutical, Biotechnology, CRO, or Clinical Research Industry.

  • At least 2 years of experience in Medical Writing or Safety Writing.

Industry Knowledge

  • Strong understanding of:

    • Pharmacovigilance

    • Drug Safety

    • Aggregate Reporting

    • Signal Detection

    • Risk Management

    • Regulatory Documentation

  • Knowledge of:

    • ICH Guidelines

    • Good Pharmacovigilance Practices (GVP)

    • Good Clinical Practice (GCP)

    • Global Regulatory Requirements