Bristol Myers Squibb Hiring Clinical Data Manager & Senior CDM | Hyderabad

Bristol Myers Squibb Hiring Clinical Data Manager & Senior CDM | Hyderabad
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Bristol Myers Squibb Hiring Clinical Data Manager & Senior CDM | Hyderabad Jobs

🏢 Bristol Myers Squibb
📍 Hyderabad, Telangana, India
🎓 B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Biotech
💼 CDM: 2+ Years | Senior CDM: 4+ Years
💻 Hybrid / Office-Based Models

Are you seeking Bristol Myers Squibb Careers or Clinical Data Manager Jobs in Hyderabad? Global biopharmaceutical giant Bristol Myers Squibb (BMS) has announced recruitment for Clinical Data Manager and Senior Clinical Data Manager positions at its Hyderabad, India facility.

These clinical data management vacancies are ideal for pharmacy and life sciences professionals with experience in Electronic Data Capture (EDC) systems, Medidata RAVE, external vendor data review, and clinical database locking. To align your clinical research resume for this selection process, read our guide on how to apply for healthcare and pharma jobs online.

📋 Job Highlights

Particular Details
Company Bristol Myers Squibb (BMS Business Services India Pvt Ltd)
Open Positions Clinical Data Manager | Senior Clinical Data Manager
Job Requisitions CDM: R1602847-1 | Senior CDM: R1602848-1
Job Location Hyderabad, Telangana, India
Department Global Clinical Data Management (CDM)
Employment Type Full-Time
Experience Required CDM: Relevant CDM experience preferred (2-4 yrs) | Senior CDM: 4+ Years
Qualifications Bachelor's or Master's Degree in Life Sciences, Pharmacy, or Biotechnology
Estimated Salary As Per Industry Benchmarks (Based on experience)
Last Date to Apply Senior CDM: July 3, 2026 | CDM: July 7, 2026

💼 Key Responsibilities

1. Clinical Data Manager (CDM)

  • Protocol Review: Understand and review clinical study protocols alongside Protocol Data Review Plans (PDRP) and Data Quality Management Plans (DQMP).
  • Data Cleaning: Review clinical data listings, perform query management, and execute data cleaning according to defined Clean Patient Group criteria.
  • Milestone Coordination: Perform CRF/field freezing and database locking activities, working in coordination with the Data Management Lead.
  • External Data Management: Track external clinical data loads, review external data listings, and address discrepancies with external vendors.
  • Audit Readiness: File study-specific documents in the electronic Trial Master File (eTMF) in compliance with the eTMF Master Plan.

2. Senior Clinical Data Manager (Senior CDM)

  • Leadership & Review: Lead end-to-end data review processes, prioritize critical data paths, and formulate inputs for study Data Review Plans.
  • Complex Datasets: Review complex external clinical datasets including Blinded Independent Committee Review (BICR), Biomarker, and SAE data.
  • Mentorship: Provide functional training and mentorship to junior clinical data management team members.
  • Regulatory Compliance: Ensure all data operations comply with FDA, ICH-GCP, and local regulatory standards.

To learn how clinical data management salaries compare to pharmacovigilance and drug safety associate structures in global pharma companies, read our report on Pharmacovigilance Salary: India vs USA.

🎓 Required Qualifications & Skills

  • Education: Bachelor's or Master's degree in Life Sciences, Pharmacy (B.Pharm, M.Pharm, Pharm.D), Biotechnology, or other relevant healthcare disciplines.
  • Experience:
    • Clinical Data Manager: Relevant clinical data review and cleaning experience is preferred (typically 2+ years).
    • Senior Clinical Data Manager: Minimum 4 years of clinical data review experience.
  • Systems: Strong experience working with EDC platforms (Medidata RAVE is preferred) and maintaining essential documents in eTMF.
  • Technical Skills: Proficient in clinical drug development processes, FDA guidelines, and GCP guidelines. High proficiency in MS Office tools.

For pharmacy graduates evaluating data management career pathways compared to laboratory drug discovery tracks, read our analysis on B.Pharm Careers after Graduation: India vs USA.

🎁 Why Join Bristol Myers Squibb?

  • Work with a leading global biopharmaceutical company dedicated to treating serious diseases.
  • Gain exposure to complex multi-indication oncology and immunology clinical pipelines.
  • Hybrid working environment (eligibility for up to 50% remote work over a 2-week period for design roles).
  • Strong career progression, global cross-functional collaboration, and competitive benefits.

To evaluate your basic knowledge of clinical trials, protocol definitions, and GCP terms before your screening, try our interactive Clinical Trial Assistant (CTA) Quiz.

💡 Clinical Data Management vs Healthcare IT

Clinical Data Managers review patient registries, resolve database queries, and manage external data streams to ensure clinical database integrity, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.

📝 Resume Tips for BMS CDM Candidates

  • Detail EDC and RAVE Tools: Explicitly mention your hands-on experience with Medidata RAVE or other clinical trial database interfaces.
  • Highlight Specific Datasets Reviewed: For senior roles, highlight experience reviewing biomarker, pharmacokinetic (PK), or SAE datasets.
  • Showcase Data Locking Achievements: Mention the number of study databases you have successfully helped clean, freeze, and lock within milestones.

💬 BMS Clinical Data Manager Interview Questions

  • Q1. What is a Data Quality Management Plan (DQMP) and why is it used?
    Answer Guidance: The DQMP defines the strategies, roles, and automated checks used to ensure clinical database accuracy, outlining how data queries are raised, resolved, and documented throughout the study.
  • Q2. How do you handle discrepancies in external vendor data like laboratory values or biomarkers?
    Answer Guidance: I compare external datasets against database listings to locate mismatches in subject IDs or dates. I then raise a data clarification query to the external vendor or site, track the response, and coordinate the reload.
  • Q3. Explain the difference between freezing and locking a case report form (CRF).
    Answer Guidance: Freezing prevents investigator sites from editing data while data management performs cleaning and review. Locking is the final step, removing all edit access permanently once the database is declared clean and complete.

🚀 How to Apply?

Interested and eligible candidates can submit their applications directly via Bristol Myers Squibb's official Workday portal:

Apply Online – Clinical Data Manager (R1602847-1) Apply Online – Senior Clinical Data Manager (R1602848-1)

⏰ Deadlines: Senior CDM: July 3, 2026 | CDM: July 7, 2026

❓ Frequently Asked Questions

Q. What is the experience required for the Senior CDM role at BMS?
BMS requires a minimum of 4 years of experience in clinical data review and data cleaning tasks.

Q. Is this position remote or hybrid?
This is a full-time, office-based position with site-by-design hybrid flexibility (up to 50% remote work over a 2-week period).

Q. What is the last date to apply for these Clinical Data Management positions?
The deadline is July 3, 2026, for the Senior Clinical Data Manager role, and July 7, 2026, for the Clinical Data Manager role.

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