Senior Principal Scientist, Clinical Research, Endometrial Cancer

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Base: $282,200.00 - $444,200.00; bonus/equity: eli...
Hybrid
Clinical trial design and execution
Oncology clinical research expertise
Medical oversight of clinical trials
The Senior Clinical Director is responsible for managing the entire clinical development cycle for oncology medicines, including study design, execution, analysis, and regulatory reporting

Job Summary

  • The Senior Clinical Director is responsible for managing the entire clinical development cycle for oncology medicines, including study design, execution, analysis, and regulatory reporting.
  • The role involves collaborating with cross-functional teams and external researchers, maintaining scientific knowledge, and providing expert opinions internally and externally.
  • The company offers a comprehensive benefits package including medical, dental, vision, retirement plans, paid holidays, vacation, and supports a hybrid work model for office-based employees.

Matching Summary

The Senior Clinical Director is responsible for managing the entire clinical development cycle for oncology medicines, including study design, execution, analysis, and regulatory reporting.

Salary

Base: $282,200.00 - $444,200.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, retirement, paid holidays, vacation, and sick days

Skills & Requirements

Must-have

  • Clinical trial design and execution
  • Oncology clinical research expertise
  • Medical oversight of clinical trials
  • Data analysis and regulatory reporting
  • Cross-functional team collaboration
  • Scientific research and strategic planning

Nice-to-have

  • Strong interpersonal and team skills
  • Experience with external research collaborations
  • Participation in scientific meetings
  • Business development support
  • Hybrid work environment
  • Commitment to diversity and inclusion

Key Requirements

  • M.D or M.D./Ph.D. degree
  • Minimum 3 years clinical medicine experience
  • Minimum 3 years industry drug development experience
  • Board Certified or Eligible in oncology/hematology preferred
  • Proven track record in clinical medicine and biomedical research
  • Experience overseeing clinical studies and protocols

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter