Bristol Myers Squibb Careers: Apply Now for Senior Manager
Bristol Myers Squibb Careers: Bristol Myers Squibb (BMS) is seeking an experienced and scientifically driven Senior Manager, Clinical Scientist for its Global Drug Development division in Hyderabad. This role is ideal for professionals who excel in clinical research, protocol development, medical writing, and cross-functional collaboration. Candidates who are passionate about advancing transformative therapies and contributing to life-changing science will find this opportunity both meaningful and career-defining.
Bristol Myers Squibb Careers Job Details
- Position: Senior Manager, Clinical Scientist
- Location: Hyderabad – Telangana
- Department: R&D / Global Drug Development
- Work Model: On-site / Hybrid (Site-by-Design—minimum 50% on-site required)
- Travel: Domestic and international travel may be required
Bristol Myers Squibb Careers: About the Company
Bristol Myers Squibb is a global biopharmaceutical leader dedicated to transforming patients’ lives through science™. The company is known for its pioneering work in oncology, immunology, hematology, cell therapy, and cardiovascular diseases. At BMS, employees experience a uniquely collaborative and mission-driven culture where curiosity, innovation, and scientific excellence power every breakthrough. The organization encourages flexibility, balance, and access to competitive benefits while enabling employees to grow through unmatched global opportunities.
Qualifications & Experience
Educational Requirements
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An MD in Pharmacology is preferred.
Experience Requirements
- Strong foundational knowledge of GCP/ICH guidelines, drug development, protocol design, and clinical operations.
- Ability to interpret protocol requirements and provide scientific input.
- Intermediate medical writing and data review capabilities.
- Basic project management and planning skills.
About the Role
The senior manager, a clinical scientist, plays a critical role in designing and executing clinical trials, supporting clinical strategy, and ensuring the scientific integrity of assigned studies. The position partners closely with cross-functional teams, medical experts, clinical operations, and data management groups to deliver high-quality clinical studies across global development programs.
Key Responsibilities
Clinical Trial Design & Execution
- Contributes to the planning, design, and delivery of assigned clinical studies.
- May serve as clinical trial lead for one or more trials.
- Co-leads study team meetings with the GDO Protocol Manager.
Scientific & Document Development
- Develops and reviews protocols, Informed Consent Forms (ICFs), amendments, and related clinical documents.
- Conducts literature reviews and supports clinical data interpretation.
- Provides scientific inputs to Clinical Study Reports (CSRs) and regulatory documents such as IBs, DSURs, PSURs, and agency responses.
Cross-Functional Collaboration
- Partners with key stakeholders, including KOLs, investigators, regulatory, operations, and data management teams.
- Develops site and CRA training materials; presents at SIVs and investigator meetings.
- Monitors clinical data and supports trend identification and data quality oversight.
Data & Quality Oversight
- Develops Data Review Plans collaboratively with Data Management.
- Ensures CRF design supports accurate data capture aligned with protocol requirements.
- Submits clinical documents to TMF and ensures documentation completeness.
Operational Excellence
- Supports program-specific data reviews, contributes to problem-solving, and maintains clear communication with management.
- Applies best practices and adheres to compliance, quality, and GCP/ICH regulations.
