Director, Clinical Science

Added
18 days ago
Type
Full time
Salary
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gcp clinical trials clinical data analysis medical writing regulatory submissions
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πŸ“‹ Description

  • Support the design, implementation, and oversight of clinical studies, including human pharmacology
  • Contribute to clinical data analysis, interpretation, and reporting, with a focus on evaluating
  • Collaborate with multidisciplinary study teams to ensure clinical activities are conducted in
  • Provide scientific leadership for clinical reports, data analysis reports, presentations, clinical
  • Contribute to regulatory submissions and interactions, including INDs, NDAs, BLAs, regulatory
  • Support the development of clinical and scientific rationales, benefit-risk assessments, efficacy

🎯 Requirements

  • PhD, PharmD, and/or MD in a relevant life science or healthcare discipline.
  • 6+ years of pharmaceutical industry experience, with equivalent combinations of education and
  • Demonstrated experience working on clinical trials and clinical studies; experience with human
  • Experience in rare disease and/or nephrology is strongly preferred.
  • Experience contributing to regulatory submissions such as INDs, NDAs, and BLAs, as well as
  • Strong scientific expertise and the ability to review, interpret, and communicate complex clinical

🎁 Benefits

  • Target base salary range of $206,000–$268,000, with actual compensation determined by experience
  • Short-term incentive compensation opportunities.
  • Long-term incentive compensation, including company stock.
  • Premium health benefits for eligible employees and dependents.
  • Financial and retirement benefits, including a retirement plan with employer matching.
  • Life insurance and disability coverage.
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