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PHARMA JOBS POST > Bristol Myers Squibb Hiring Safety Narrative Writer in Hyderabad | Apply Now

Bristol Myers Squibb Hiring Safety Narrative Writer in Hyderabad | Apply Now

Bristol Myers Squibb is hiring Safety Narrative Writers in Hyderabad. Candidates with 2–5 years of experience in clinical documentation, medical writing, pharmacovigilance, or clinical research can apply now.

ADMIN
Last updated: June 23, 2026 5:16 am
ADMIN 3 weeks ago
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Bristol Myers Squibb Hiring Safety Narrative Writer in Hyderabad
Bristol Myers Squibb Hiring Safety Narrative Writer in Hyderabad
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  • Hyderabad, Telangana, India
  • Posted 3 weeks ago
Bristol Myers Squibb

Bristol Myers Squibb

Bristol Myers Squibb (BMS) is hiring experienced professionals for the position of Safety Narrative Writer in Hyderabad, Telangana. This is an excellent opportunity for life sciences professionals with experience in clinical documentation, pharmacovigilance, medical writing, or clinical research to join a global biopharmaceutical leader dedicated to transforming patients’ lives through science.

Job Details

Position: Safety Narrative Writer
Location: Hyderabad, Telangana, India
Company: Bristol Myers Squibb (BMS)
Experience Required: 2–5 Years
Qualification: Bachelor’s or Master’s Degree in Biomedical, Life Sciences, Pharmacy, Biotechnology, or related fields

Key Responsibilities

  • Write, edit, review, finalize, and track Clinical Study Report (CSR) patient safety narratives.
  • Serve as the primary contact for narrative writing activities for assigned studies.
  • Ensure timely delivery and resolution of narrative-related issues.
  • Prepare accurate and medically coherent patient safety narratives using Clinical and Safety Database outputs.
  • Conduct quality control reviews, document compilation, and formatting activities.
  • Support process improvement initiatives related to patient safety narrative development.
  • Maintain high standards of quality and regulatory compliance throughout documentation processes.

Required Qualifications

  • Bachelor’s or Master’s degree in Biomedical Sciences, Life Sciences, Pharmacy, Biotechnology, or related disciplines.
  • 2–5 years of experience in clinical documentation, medical writing, pharmacovigilance, or clinical research.
  • Experience in pharmaceutical, biotechnology, or contract research organizations (CROs).
  • Basic understanding of global regulatory requirements including FDA and ICH guidelines.
  • Knowledge of drug development processes and electronic Common Technical Document (eCTD) requirements.
  • Strong ability to summarize medical data accurately and create concise, high-quality narratives.
  • Experience with electronic document management systems and PDF annotation tools.
  • Excellent organizational, communication, and time-management skills.
  • Ability to collaborate effectively within cross-functional and matrix-based teams.

Why Join Bristol Myers Squibb?

At Bristol Myers Squibb, employees work on meaningful projects that directly impact patients’ lives worldwide. The company offers:

  • Competitive compensation and benefits
  • Career growth and learning opportunities
  • Collaborative and inclusive work culture
  • Exposure to global clinical development programs
  • Flexible and supportive work environment

Work Model

The role follows Bristol Myers Squibb’s occupancy structure and may require onsite or hybrid working arrangements depending on business requirements.

If you have experience in clinical documentation, medical writing, safety narratives, pharmacovigilance, or clinical research and are looking to advance your career with a globally recognized pharmaceutical organization, apply for the Safety Narrative Writer position at Bristol Myers Squibb today.

APPLY HERE

To apply for this job please visit bristolmyerssquibb.wd5.myworkdayjobs.com.

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By ADMIN
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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
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