Scientific Director, Oncology Clinical Development

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1 hour ago
Type
Full time
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gcp clinical trials pharmacovigilance regulatory submissions regulatory
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๐Ÿ“‹ Description

  • Oversees direction, planning, execution and interpretation of clinical trials or research
  • Participates in cross-functional teams to deliver high-quality clinical data for strategy.
  • Design and implement clinical development programs and monitor study timelines.
  • Provide in-house clinical expertise for molecule and disease, coordinate activities with
  • Engage with investigators, sites, and medical affairs to integrate cross-functional perspectives.

๐ŸŽฏ Requirements

  • Bachelors in sciences; advanced degree preferred.
  • 5+ years of clinical trial experience in pharma/academia.
  • Ability to oversee a global clinical research program with minimal supervision.
  • Strong cross-functional collaboration and external/internal interaction skills.
  • Knowledge of clinical trial methodology, regulatory/compliance, and study design.
  • Excellent oral and written English communication.

๐ŸŽ Benefits

  • Comprehensive benefits package including paid time off and medical/dental/vision insurance.
  • 401(k) to eligible employees; long-term incentive programs.
  • Equal opportunity employer; commitments to integrity and innovation.
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