Clinical Program Director

7 days ago


California, United States EPM Scientific Full time
Clinical Program Lead Job Description

We are seeking a highly motivated and experienced Clinical Program Lead to join our team at EPM Scientific. As a Clinical Program Lead, you will be responsible for managing a Phase III global study and leading the design, monitoring, data interpretation, and reporting activities related to the conduct of clinical studies.

Key Responsibilities:

  • Manage a Phase III global study and lead the design, monitoring, data interpretation, and reporting activities related to the conduct of clinical studies.
  • Implement processes and initiatives to support the clinical program and study delivery, driving overall portfolio delivery.
  • Support the Director, Global Clinical Affairs in clinical operations.
  • Oversight and execution of scientific components of the program, including scientific literature review, protocol development, and Quality by Design principles.
  • Study Monitoring, oversight of data quality, patient safety, data management/cleaning activities, and clinical sites.
  • Direct reports within the Clin Ops team.

Requirements:

  • Experience establishing and/or managing a clinical trial program in the EU.
  • 3+ years of sponsor experience.
  • 2+ years of experience managing studies or trials in the EU.
  • 2+ years of on-site monitoring experience.
  • A Bachelor's degree in Biological Sciences, Nursing, Pharmacy, or a related discipline.
  • A working knowledge of ICH GCP guidelines.

What We Offer:

  • Competitive salary with benefits.
  • High degree of commercial exposure early in your career.
  • Being part of a team whose work directly aims to improve the quality of people's lives.
  • Great work-life balance.

We are an equal opportunities employer and welcome applications from all qualified candidates. If you are interested in this Clinical Program Lead role, please don't hesitate to reach out.



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