Director, Clinical Science

138804
  • 200000 USD - 200000 USD
  • Hayward, United States
  • Permanent
 We are seeking a passionate and experienced  Director of Clinical Science to play a pivotal role in our client's cutting-edge medium size biotechnology company. As a key contributor to their scientific, clinical, and operational endeavors, you'll be at the forefront of driving the success of our clinical development programs. Our client has multiple studies in solid tumor spanning from early to late development with a variety of different modalities.
 

Our client pushing the boundaries of biotechnology to bring life-changing therapies to patients around the world by utilizing precision combination therapies.  

Your Responsibilities: As the Director of Clinical Science, you'll be a driving force in the design, planning, and implementation of study protocols for our innovative investigational products. Your role will encompass a wide array of responsibilities, including:

  • Collaborating with cross-functional teams to oversee clinical studies, ensuring operational feasibility and effective data management.
  • Conducting medical and safety data reviews, providing insightful analyses, and offering preliminary assessments.
  • Supporting data review committees and communicating synthesized data reports.
  • Authoring clinical documents, protocols, study reports, and more.
  • Engaging with internal and external stakeholders to drive program-level development strategies.
  • Serving as a recognized clinical expert for assigned programs.
  • Contributing to scientific publications, abstracts, and presentations.
  • Managing and mentoring junior clinical scientists.

Qualifications and Requirements: Your expertise and enthusiasm will be critical to our success. To excel in this role, you should bring:

  • A PhD in a health science field, PharmD, MD, or relevant advanced degree.
  • A minimum of 5+ years of experience for Director
  • Experience in oncology or oncology immunotherapy clinical trials, with a preference for lung cancer trials.
  • Proficiency in late-stage drug development.
  • Strong analytical skills and a grasp of safety and pharmacovigilance principles.

Why

  • Competitive salary range, along with stock programs and performance-based bonuses.
  • Comprehensive benefits package to support your well-being.
  • Opportunity to work on groundbreaking therapies that make a real difference.
  • A dynamic and collaborative work environment that values innovation and teamwork.
Thomas Huynh Resourcer

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