EU Clinical Program Director

18 hours ago


London, Greater London, United Kingdom EPM Scientific Full time

At EPM Scientific, we are seeking a highly skilled Clinical Program Lead to support our team in Surrey. This is a competitive salary with benefits opportunity to contribute to a team whose work directly benefits healthcare and strives to improve people's lives.

About the Role

The successful candidate will be responsible for designing, monitoring, data interpretation, and reporting related to the conduct of interventional and/or non-interventional clinical studies. This includes building expertise and staying up-to-date in the scientific aspects of the program, e.g., scientific literature review.

  • Supporting the Director, Global Clinical Affairs in implementing the vision for Clinical Affairs to drive the quality, cost, speed, and efficiency of clinical studies delivery.
  • Implementing the program strategy and contributing to the overall strategy of the Clinical Affairs department alongside other Clinical Program Leads.

The estimated salary for this role is £80,000 - £110,000 per annum, depending on experience.

Key Responsibilities

The Clinical Program Lead will be responsible for:

  • Clinical Program Delivery
    • Protocol development and implementation of Quality by Design principles.
    • Study monitoring, oversight of data quality and integrity, and ensuring the safety and rights of participants.
  • Clinical Program Enabling Activities
    • Implementing activities and initiatives that support program and study delivery and overall portfolio efficiency.
  • People Management
    • Providing leadership, support, feedback, coaching, and mentoring to the core Study Management Team.
Requirements

To be considered for this role, you must have:

  • Graduate qualifications in Biological Sciences, Nursing, Pharmacy, or Medicine (post-graduate qualifications desirable).
  • Working knowledge of international clinical research regulations and requirements, including ICH/GCP guidelines.
  • Proven experience in the management of clinical trials in the EU.

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