Clinical Project Manager (NASH)

  • 80000 EUR - 80000 EUR
  • europe, United Kingdom
  • Permanent

Job Title: Clinical Project Manager - NASH Therapy

Company: Global (CRO)

Location: Remote

About Us:

A leading global Contract Research Organization (CRO) dedicated to advancing pharmaceutical and biotech research to improve patient outcomes worldwide. Our diverse team of experts collaborates with clients to deliver innovative solutions throughout all phases of clinical development.

Position Overview:

We are seeking a talented and experienced Clinical Project Manager (CPM) with expertise in Nonalcoholic Steatohepatitis (NASH) therapy to join our dynamic team. As a Clinical Project Manager, you will play a crucial role in overseeing and managing clinical trials focused on NASH therapy, ensuring successful execution from initiation to closeout.


Key Responsibilities:

  • Lead and manage clinical trials focused on NASH therapy, ensuring adherence to protocol, regulatory requirements, and timelines.
  • Develop and oversee project plans, including timelines, budgets, and resource allocation.
  • Coordinate and communicate effectively with cross-functional teams, including investigators, sponsors, vendors, and internal stakeholders.
  • Monitor study progress and proactively identify and address potential risks or issues.
  • Collaborate with the clinical team to ensure data integrity and quality throughout the trial.
  • Serve as the primary point of contact for all NASH therapy-related matters, providing leadership and guidance to the project team.
  • Contribute to the development of study protocols, informed consent forms, and other study-related documents.
  • Participate in site selection, initiation, and closeout activities as needed.
  • Stay current with industry trends, regulatory guidelines, and therapeutic developments related to NASH therapy.


  • Bachelor's degree in life sciences or a related field; advanced degree preferred.
  • Minimum of 3+ years of experience in clinical project management, with a focus on NASH therapy.
  • Proven track record of successfully managing clinical trials from start to finish.
  • Strong understanding of clinical trial operations, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Why Join Us:

If you are passionate about NASH have a proven track record as a CPM, and are ready to take on a challenging and rewarding role, we encourage you to apply.

Laurie Watts Lead Client Partner

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