Senior Manager – Clinical Scientist
Location: Hyderabad, Telangana, India
Experience Required: 5+ Years
Job Type: Full-Time
Job ID: R1597648
About Bristol Myers Squibb (BMS)
Bristol Myers Squibb (BMS) is a global biopharmaceutical leader committed to transforming patients’ lives through science™. With groundbreaking innovations across oncology, immunology, cardiovascular, and other therapeutic areas, BMS empowers its teams to deliver life-changing therapies while fostering a culture of passion, innovation, inclusion, and accountability.
Role Overview
The Senior Manager, Clinical Scientist will provide scientific and clinical expertise to early-phase and ongoing clinical trials. This role involves medical monitoring, data review, cross-functional collaboration, and clinical document development, ensuring regulatory compliance and high-quality outcomes. The role offers exposure to global clinical operations, regulatory interactions, and strategic planning for clinical development programs.
Key Responsibilities
Clinical Oversight & Monitoring
Conduct medical monitoring of assigned clinical studies, ensuring patient safety and data integrity.
Review clinical narratives, case report forms (CRFs), and clinical study reports (CSRs).
Identify trends in clinical data and support Data Review Plan development.
Protocol & Regulatory Support
Collaborate cross-functionally to develop, review, and amend Protocol and Informed Consent Form (ICF) documents.
Contribute clinical insights for regulatory submissions including Pre-IND, IND, IB, DSUR, PSUR, and orphan drug reports.
Submit clinical documents to Trial Master File (TMF) and ensure documentation compliance.
Medical Communication & Training
Conduct literature reviews and synthesize clinical evidence for internal and external stakeholders.
Develop and deliver training materials for sites, CRAs, and investigator meetings.
Serve as a scientific liaison with external partners including Key Opinion Leaders (KOLs).
Collaboration & Cross-Functional Support
Work closely with Clinical Operations, Data Management, Regulatory, and Safety teams.
Ensure CRF design supports protocol-aligned data collection.
Support establishment of Data Monitoring Committees, dose review teams, and adjudication committees.
Required Qualifications & Skills
Education: MD, MBBS, DM, PharmD, PhD, or equivalent in Life Sciences.
Experience: 5+ years in clinical research, clinical science, or related roles.
Medical Monitoring: Proven experience in early-phase clinical trials.
Regulatory Knowledge: Proficient in GCP, ICH guidelines, study design, drug development processes, and clinical operations.
Technical Skills: Intermediate proficiency in Microsoft Word, Excel, PowerPoint, and clinical data review tools.
Core Competencies: Critical thinking, problem-solving, attention to detail, adaptability, and effective cross-functional collaboration.
Communication: Strong written and verbal communication skills; capable of presenting complex scientific information to varied audiences.
Travel: Domestic and international travel may be required (10–25%).
Why Join BMS
Work on innovative clinical programs that impact patient care globally.
Collaborate with high-performing teams in a supportive and inclusive environment.
Access opportunities for professional growth and leadership development.
Contribute to transformational therapies in oncology, immunology, and other therapeutic areas.
Equal Opportunity & Accessibility
BMS is committed to diversity, equity, and inclusion. Applicants with disabilities may request reasonable accommodations during the recruitment process. BMS provides a transparent and secure application process, ensuring no payments or financial information is ever requested.
Apply Now to join BMS and be part of a team transforming patient lives through science.
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