Scientific Director, Oncology Early Development

Added
10 days ago
Type
Full time
Salary
Upgrade to Premium to se...

Related skills

gcp regulatory affairs clinical trial pharmacovigilance oncology

๐Ÿ“‹ Description

  • Manages the design and implementation of one or more clinical development programs in support of an
  • Has overall responsibility for oversight of 1-2 clinical studies, monitoring overall study
  • Responsible for design, analysis, interpretation, and reporting of scientific content of protocols
  • May oversee the work of Associate Scientific Directors and/or of Clinical Scientists working on the
  • Provides in-house clinical expertise for the molecule and disease, coordinating appropriate
  • Will serve on an Asset Study Team (AST), with responsibility for development of a rigorous

๐ŸŽฏ Requirements

  • Bachelors degree in the sciences; advanced degree (e.g., MS, PhD, PharmD) preferred
  • Ability to provide input and direction to clinical research with appropriate supervision
  • At least 5+ years of clinical trial experience in the pharmaceutical industry, academia, or
  • Ability to oversee a clinical research program of moderate complexity with minimal supervision
  • Ability to perform and bring out the best in others on a cross-functional global team
  • Ability to interact externally and internally to support a global scientific and business strategy

๐ŸŽ Benefits

  • Comprehensive package of benefits including paid time off (vacation, holidays, sick)
  • Long-term incentive programs
Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Healthcare Jobs. Just set your preferences and Job Copilot will do the rest โ€” finding, filtering, and applying while you focus on what matters.

Related Healthcare Jobs

See more Healthcare jobs โ†’