MD Job at Bristol Myers Squibb | Senior Clinical Scientist Role
Bristol Myers Squibb is offering an excellent MD Job opportunity in Hyderabad for experienced medical professionals interested in global drug development. This medical job is ideal for MD-qualified candidates looking to work as a Senior Manager, Clinical Scientist, contributing to impactful clinical research and advancing patient-focused therapies through Bristol Myers Squibb jobs.
MD Job Details:
- Job Title: Senior Manager, Clinical Scientist
- Division: R&D / Global Drug Development
- Location: Hyderabad, Telangana, India
About the Company
Working at Bristol Myers Squibb means being part of a challenging, meaningful, and life-changing work environment. This global biopharmaceutical leader offers impactful medical jobs that contribute to innovative therapies, including advancements in cell therapy and global drug development. Bristol Myers Squibb jobs provide opportunities to grow, thrive, and build long-term careers while maintaining balance and flexibility through competitive employee benefits and programs.
Qualifications:
Degree(MD, PhD). MD-Pharmacology preferred.
Experience Requirements
- Basic knowledge of GCP/ICH, drug development process, study design, statistics, and clinical operations
- Ability to understand assigned protocol(s) and their requirements
- Basic knowledge and skills to support program-specific data review and trend identification
- Intermediate medical writing skills and medical terminology
- Basic planning/project management skills (develop short-range plans that are realistic and effective)
MD Job Position Summary / Objective
This MD Job will be responsible for the design and execution of assigned clinical trial activities and will work closely with cross-functional teams within the assigned project. The role may serve as Clinical Trial Lead for one or more trials and co-lead study team meetings in partnership with the GDO protocol manager. This senior medical job supports high-impact clinical programs at Bristol Myers Squibb.
Key Responsibilities
- Collaborate and liaise with external partners, including KOLs
- Seek out and implement best practices in clinical research
- Provide timely updates to management
- Develop Protocol and ICF documents and amendments
- Conduct literature reviews to support clinical strategies
- Submit clinical documents to the TMF
- Develop and deliver site and CRA training materials
- Review clinical narratives and monitor data trends
- Develop Data Review Plans with Data Management
- Ensure CRF design aligns with protocol requirements
- Contribute to CSRs and regulatory documents, including IB, DSUR, PSUR, and regulatory submissions
