About the Company
Bristol Myers Squibb (BMS) is a globally recognized biopharmaceutical company dedicated to transforming patients’ lives through innovative science.
With a strong presence across multiple countries, BMS develops life-changing medicines in oncology, hematology, immunology, cardiovascular diseases, and other therapeutic areas.
The company is known for maintaining high regulatory standards while following global guidelines from organizations such as the FDA and ICH.
BMS fosters a collaborative, inclusive, and innovation-driven work environment where employees are empowered to grow professionally while contributing to meaningful healthcare advancements worldwide.
Job Details
- Company Name: Bristol Myers Squibb (BMS)
- Position: Clinical Data Manager
- Experience: Minimum 2 years
- Qualification: Bachelor’s Degree (Life Sciences, Pharmacy, or relevant field preferred)
- Location: Hyderabad, Telangana, India
- Work Type: Full-Time, Hybrid (Site-by-Design with minimum 50% onsite)
Job Description
Bristol Myers Squibb is seeking an experienced Clinical Data Manager to support clinical development programs by ensuring high-quality clinical data management and review.
The selected candidate will work with cross-functional global teams to maintain accurate, compliant, and timely clinical trial data.
Clinical Data Manager
- Department: Clinical Data Management
- Market: Global Clinical Development
- Role: Clinical Data Manager
- Experience: Minimum 2 years in Clinical Data Review
- Education/Qualification: Bachelor’s Degree; Life Sciences, Pharmacy, or related discipline preferred
Skills/Qualifications
- Bachelor’s Degree in Life Sciences, Pharmacy, or related discipline.
- Minimum two years of clinical data review experience.
- Knowledge of the clinical drug development process.
- Understanding of FDA and ICH guidelines.
- Experience with Electronic Data Capture (EDC) systems.
- Hands-on knowledge of Medidata RAVE preferred.
- Strong Microsoft Office skills.
- Excellent written and verbal communication.
- Ability to collaborate with multidisciplinary teams.
- Strong analytical and problem-solving abilities.
- Good documentation and data review skills.
- Attention to detail and regulatory compliance.
Key Responsibilities
- Review study protocols and data review documents.
- Perform clinical data review activities.
- Identify and resolve data discrepancies.
- Execute data cleaning activities.
- Freeze and lock CRFs and fields.
- Coordinate study deliverables with Data Management Lead.
- Review loaded external clinical data.
- Track external data loads.
- Resolve vendor-related data discrepancies.
- Maintain documentation in eTMF.
- Ensure compliance with data management plans.
- Support quality clinical trial execution.
Benefits/Perks
- Competitive salary and employee benefits.
- Career growth with a global biopharmaceutical leader.
- Learning and professional development opportunities.
- Exposure to international clinical research projects.
- Inclusive and collaborative workplace.
- Flexible hybrid work model.
- Opportunity to work with advanced clinical technologies.
- Strong focus on employee wellbeing.
- Innovative and science-driven culture.
- Long-term career advancement opportunities.
How to Apply
Interested candidates can apply directly through the official Bristol Myers Squibb Careers portal.
Official Careers Page: https://careers.bms.com/
Applicants should prepare an updated resume highlighting their clinical data management experience, regulatory knowledge, and proficiency with EDC platforms such as Medidata RAVE.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Bristol career page.

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Apply today and take the next step toward building a rewarding global career with Bristol Myers Squibb.
Why You Should Join Bristol Myers Squibb
Bristol Myers Squibb offers an exceptional opportunity to work on life-changing clinical research while collaborating with global healthcare professionals. Employees benefit from a culture built on innovation, integrity, accountability, inclusion, and continuous learning.
The company provides exposure to international clinical development projects, advanced technologies, and structured career progression.
Working at BMS allows professionals to contribute to meaningful scientific discoveries while building long-term career stability in a highly regulated pharmaceutical environment.
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