MD Pharmacology Job | Bristol Myers Squibb Hiring – Apply Now
If you’re searching for a high-impact MD Pharmacology job that blends scientific expertise with innovative clinical research, this Senior Manager, Clinical Scientist role at Bristol Myers Squibb in Hyderabad is an excellent opportunity. As part of Bristol Myers Squibb careers, this position offers meaningful work, career growth, and exposure to global drug development, ideal for professionals looking to build a future in a transformational clinical job.
Job Details:
- Job Title: Senior Manager, Clinical Scientist
- Division: R&D / Global Drug Development
- Job Position: Senior Manager – Clinical Scientist
- Location: Hyderabad, Telangana, India
About the Company
Bristol Myers Squibb is a global biopharmaceutical leader offering transformative opportunities through its diverse portfolio. As a part of Bristol Myers Squibb careers, employees contribute to challenging, meaningful, and life-changing work across clinical, research, and development functions. The company supports a flexible environment and provides competitive benefits that help employees pursue both personal and professional goals.
Qualifications and Experience Requirements
- MD-Pharmacology preferred
- Basic knowledge of GCP/ICH and drug development processes.
- Understanding of assigned protocols and their requirements.
- Skills for program-specific data review and trend detection.
- Intermediate medical writing skills and medical terminology.
- Basic planning and project management capability.
MD Pharmacology Job Description
The Senior Manager, Clinical Scientist will support the design and conduct of assigned clinical trials. Responsibilities include working closely with clinical team members, ensuring seamless study execution, serving as Clinical Trial Lead when required, co-leading study team meetings, and collaborating with cross-functional teams. This role aligns well with professionals pursuing an MD Pharmacology job within an innovative organization.
MD Pharmacology Job – Key Responsibilities
- Collaborate and liaise with external partners (e.g., KOLs).
- Seek out and enact best practices with guidance.
- Provide regular and timely updates to management.
- Develop Protocol and ICF documents, amendments, and present to governance committees.
- Conduct literature review.
- Submit clinical documents to TMF.
- Develop site and CRA training materials and present during SIVs and Investigator Meetings.
- Review clinical narratives.
- Monitor clinical data and trends.
- Develop Data Review Plan with Data Management.
- Ensure CRF design supports accurate data collection per protocol.
- Contribute to CSRs and regulatory documents (IB, DSUR, PSUR, Orphan Annual Reports, HA/EC/IRB responses).
