Associate Director, Senior Clinical Scientist

Bristol Myers Squibb

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Clinical trial lead responsibilities
Local health authority interactions
Protocol and icf development
** Bristol Myers Squibb is seeking an Associate Director, Senior Clinical Scientist to lead and manage clinical trial activities, particularly in oncology and hematology. The role requires extensive experience in clinical science and the ability to collaborate with cross-functional teams, offering a dynamic work environment with competitive benefits. **

Job Summary

  • Responsible for implementation, planning, and execution of assigned clinical trial activities and serves as Clinical Trial Lead for one or more trials.
  • Provides scientific and clinical leadership to the team of supporting Clinical Scientists and collaborates with cross-functional study team members.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment and offers a wide variety of competitive benefits, services and programs.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking an Associate Director, Senior Clinical Scientist to lead and manage clinical trial activities, particularly in oncology and hematology. The role requires extensive experience in clinical science and the ability to collaborate with cross-functional teams, offering a dynamic work environment with competitive benefits. **

Skills & Requirements

Must-have

  • Clinical trial lead responsibilities
  • Local health authority interactions
  • Protocol and ICF development
  • Clinical data review and trend identification
  • GCP/ICH and drug development process knowledge

Nice-to-have

  • Adaptable and flexible
  • Strong sense of teamwork
  • Critical thinking and problem-solving

Key Requirements

  • 10+ years of experience in clinical science
  • Medical qualification (MD preferred)
  • Experience in Oncology and Hematology therapeutic areas preferred
  • Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations
  • Experience leading scientific interactions with DCGI and Subject Expert Committees

Work Rights

Not specified

Tailored Resume

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