BMS Hiring Safety Narrative Writer | Hyderabad
Bristol Myers Squibb Hiring Safety Narrative Writer | Life Sciences Jobs in Hyderabad
Professionals seeking medical writing jobs in Hyderabad, clinical documentation careers, or pharmacovigilance writing opportunities can explore this latest opening from Bristol Myers Squibb (BMS). The company is currently hiring for the position of Safety Narrative Writer at its Hyderabad location.
This opportunity is ideal for candidates with experience in clinical documentation, pharmacovigilance, drug safety, clinical research, medical writing, and biotechnology operations. Candidates from Life Sciences, Pharmacy, Biotechnology, and Biomedical backgrounds with strong medical writing and data interpretation skills are encouraged to apply.
As global pharmaceutical companies continue expanding drug development and patient safety programs, Safety Narrative Writers play a critical role in preparing high-quality clinical safety documentation that supports regulatory submissions and clinical study reporting.
Company Overview
Bristol Myers Squibb (BMS) is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients overcome serious diseases. Since its inception, the company has built a strong reputation in areas such as oncology, immunology, cardiovascular diseases, hematology, and cell therapy.
BMS operates across multiple countries and is recognized for its research-driven culture, commitment to scientific innovation, and focus on improving patient outcomes worldwide. The company offers employees opportunities to work on impactful projects while collaborating with global teams across clinical development, regulatory affairs, pharmacovigilance, and medical writing functions.
Job Role & Responsibilities
Position: Safety Narrative Writer
Job ID
R1603667
Key Responsibilities
The selected candidate will support clinical development programs through preparation and management of patient safety narratives and related clinical documentation.
Key responsibilities include:
- Write, edit, review, and finalize Clinical Study Report (CSR) patient safety narratives.
- Serve as the primary point of contact for narrative writing activities on assigned studies.
- Prepare medically coherent and accurate patient safety narratives using clinical and safety database outputs.
- Ensure narrative deliverables meet project timelines and quality standards.
- Conduct final quality control reviews, formatting checks, and compilation activities.
- Track narrative deliverables and resolve narrative-related issues.
- Support process improvement initiatives related to safety narrative production.
- Collaborate with multidisciplinary clinical development teams.
- Maintain documentation within electronic document management systems.
- Ensure compliance with regulatory requirements and organizational standards.
Skills Required
Candidates should possess knowledge or experience in:
- Medical Writing
- Clinical Documentation
- Pharmacovigilance
- Drug Safety
- Clinical Research
- Safety Narrative Writing
- Clinical Study Reports (CSR)
- FDA Regulations
- ICH Guidelines
- eCTD Documentation
- Quality Review Processes
- Clinical Data Interpretation
- Regulatory Compliance
- Electronic Document Management Systems
Eligibility / Qualifications
Educational Qualification
Candidates should possess any of the following:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Biomedical Sciences
- Biochemistry
- Microbiology
- Clinical Research
- Other Biomedical or Life Sciences Degrees
Experience Required
- Bachelor’s Degree with 2–5 years of relevant experience
OR - Master’s Degree with 1–3 years of relevant experience
Preferred Experience
- Clinical documentation experience
- Pharmacovigilance experience
- Clinical research experience
- Biotechnology industry experience
- Contract Research Organization (CRO) experience
- Pharmaceutical industry experience
Preferred Competencies
- Strong medical writing abilities
- Excellent written and verbal communication skills
- Ability to summarize complex medical information accurately
- Knowledge of FDA and ICH regulatory guidelines
- Understanding of drug development processes
- Familiarity with eCTD requirements
- Strong organizational and project management skills
- Attention to detail and quality compliance
Location & Salary
Location: Hyderabad, Telangana
Work Model: On-Site / Hybrid (as per company occupancy policy)
Experience: 2–5 Years
Estimated Salary: ₹6 LPA – ₹12 LPA (Approximate, based on experience, skills, and company compensation structure)
Application Process
Interested candidates can apply through the official Bristol Myers Squibb careers portal.
Application Link:
Applicants should ensure their resume highlights:
- Clinical documentation experience
- Medical writing expertise
- Pharmacovigilance knowledge
- Clinical research experience
- Regulatory compliance exposure
- Safety narrative preparation experience
Frequently Asked Questions
What is the role offered by Bristol Myers Squibb?
BMS is hiring for the position of Safety Narrative Writer in Hyderabad.
What educational qualifications are required?
Candidates with B.Pharm, M.Pharm, Pharm.D, Biotechnology, Life Sciences, Biomedical Sciences, and related qualifications can apply.
How much experience is required?
Candidates should have approximately 2–5 years of relevant experience in clinical documentation, pharmacovigilance, clinical research, or medical writing.
Is knowledge of FDA and ICH guidelines important?
Yes. Basic knowledge of FDA regulations, ICH guidelines, and drug development processes is preferred.
What are the primary responsibilities of a Safety Narrative Writer?
The role involves preparing, reviewing, editing, and finalizing patient safety narratives for Clinical Study Reports while ensuring quality and regulatory compliance.
Where is the job located?
The position is based in Hyderabad, Telangana.
Summary
| Category | Details |
|---|---|
| Company | Bristol Myers Squibb (BMS) |
| Department Vacancies | Safety Narrative Writer |
| Qualification | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, Biotechnology, Biomedical Sciences |
| Experience | 2–5 Years |
| Location | Hyderabad, Telangana |
To apply for this job please visit bristolmyerssquibb.wd5.myworkdayjobs.com.
