Added
2 hours ago
Type
Full time
Salary
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Related skills

regulatory affairs clinical trials pharmacovigilance oncology clinical development

📋 Description

  • Collaborate with senior medical leaders, drug discovery teams, translational oncology specialists
  • Design clinical trials that rigorously test translational hypotheses and establish clinical proof
  • Prepare clinical sections of key regulatory and development documents, including Investigator’s
  • Support responses to questions and requests from regulatory authorities, Institutional Review
  • Review, assess, and interpret clinical data, translating findings into clear insights for internal
  • Manage drug safety and pharmacovigilance activities for ongoing clinical trials, supporting patient

🎯 Requirements

  • MD, MD/PhD, or another relevant advanced degree.
  • Typically 5 or more years of clinical development experience in academic and/or industry settings
  • Experience working with solid tumors; breast oncology experience is preferred.
  • Familiarity with clinical trial design and execution, including protocol development, case report
  • Experience collaborating with investigative sites, including principal investigators
  • Strong clinical judgment and the ability to assess and interpret complex clinical data to inform

🎁 Benefits

  • Estimated annual base salary: $213,000–$304,000, depending on factors such as experience
  • Remote work flexibility: Remote arrangements are available for this position.
  • Meaningful patient impact: The opportunity to contribute to the development of precision oncology
  • Scientific and professional growth: Exposure to innovative drug discovery approaches and complex
  • Cross-functional collaboration: The opportunity to work with specialists across clinical medicine
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