Associate Director, Senior Clinical Scientist

Working at Bristol Myers Squibb is challenging, meaningful, and life-changing. The company offers a wide variety of competitive benefits, services, and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.

Requirements

• Participates in designing and developing clinical studies and research plans in support of asset strategy
• Provides clinical, medical, and scientific expertise to cross-functional BMS colleagues
• Liaises with Translational & Discovery Scientists and Development Teams to define dose and schedule
• Maintains a thorough understanding of assigned protocols and protocol requirements
• Plans and leads the implementation of clinical study startup/conduct/close-out activities
• Serves as an independent Medical Monitor for clinical trials from Phase 1 through Proof-of-Concept
• Conducts and oversees activities related to data generation and validation
• Identifies clinical data trends and provides trends and escalations to study physician
• Assesses key safety-related serious adverse events in partnership with Worldwide Patient Safety
• Fulfills GCP and compliance obligations for clinical conduct and maintains all required training

Benefits

• Competitive salary
• Benefits package
• Professional development opportunities
• Work-life balance
• Paid time off
• Health insurance
• Retirement plan
• Flexible work arrangements