Associate Director – Senior Clinical Scientist
Location: Hyderabad, Telangana, India
Experience Required: 10+ Years
Job Type: Full-Time
Job ID: R1595938
About Bristol Myers Squibb (BMS)
Bristol Myers Squibb (BMS) is a global biopharmaceutical leader committed to transforming patients’ lives through science™. With cutting-edge innovation in oncology, immunology, cardiovascular diseases, and other therapeutic areas, BMS empowers teams to develop life-changing therapies. Our culture emphasizes passion, innovation, inclusion, accountability, and integrity, offering employees opportunities to grow professionally while making a tangible impact on global healthcare.
Role Overview
The Associate Director, Senior Clinical Scientist will provide strategic clinical and scientific leadership across early-phase and ongoing clinical trials. This role requires leading trial-level activities, guiding clinical scientists, and ensuring high-quality data, regulatory compliance, and operational efficiency. You will collaborate with cross-functional teams including Medical Monitors, Clinical Development Leads, Data Management, and external partners to drive clinical research programs aligned with organizational goals.
Key Responsibilities
Clinical Trial Leadership
Serve as Clinical Trial Lead for assigned studies, overseeing planning, execution, and close-out activities.
Maintain a thorough understanding of study protocols and educate supporting teams on protocol requirements.
Evaluate innovative trial designs in collaboration with Medical Monitors and Clinical Development Leads.
Protocol & Regulatory Support
Collaborate on the development and review of Protocols and Informed Consent Forms (ICFs), ensuring high clinical quality.
Review clinical narratives, CSRs, and regulatory documents (IB, DSURs, regulatory responses).
Support site-facing activities including training, clinical query resolution, and serving as primary contact for clinical questions.
Data Management & Monitoring
Provide oversight on clinical data review, trend identification, CRF design, and query resolution.
Ensure consistent quality in data review by supporting Clinical Scientists and collaborating with Data Management.
Participate in Data Monitoring Committees, dose review teams, and independent adjudication committees.
Cross-Functional Collaboration
Co-lead study team meetings and coordinate with global teams.
Serve as a liaison with external scientific partners for clinical guidance and advice.
Support clinical development planning by providing data analysis and insights.
Leadership & Mentorship
Provide guidance and matrix leadership to a team of Clinical Scientists.
Mentor team members and support professional development.
Promote quality, compliance, and scientific excellence across the clinical team.
Required Qualifications & Skills
Education: MD (Pharmacology preferred), PhD, PharmD, MS, RN, or equivalent Life Sciences degree.
Experience: 10+ years in clinical research, clinical science, or related roles with medical monitoring experience.
Regulatory Knowledge: GCP, ICH, drug development, study design, and clinical operations expertise.
Medical Monitoring & Data Review: Strong capability to analyze clinical data, identify trends, and support regulatory submissions.
Leadership: Experience leading cross-functional clinical teams and mentoring junior staff.
Technical Skills: Proficient in Microsoft Word, Excel, PowerPoint, EDC systems (e.g., RAVE), J-Review, and clinical reporting tools.
Communication: Excellent verbal, written, and interpersonal skills; ability to collaborate across all organizational levels.
Travel: Domestic and international travel may be required.
Why Join BMS
Work on innovative clinical programs that impact global patient care.
Lead high-performing teams in a supportive, inclusive, and collaborative environment.
Contribute to transformational therapies across multiple therapeutic areas.
Access opportunities for professional growth, leadership development, and global exposure.
Equal Opportunity & Accessibility
BMS is committed to diversity, equity, and inclusion. Applicants with disabilities may request reasonable accommodations during the recruitment process. BMS ensures a secure and transparent application process, with no payments or financial information ever requested.
Apply Now to be part of a team transforming patient lives through science.
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Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
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Frank Scottile Blvd |Missouri :
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Sheffield |Oxfordshire :
Witney |Ontario :
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