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Clinical Project Manager

Clinical Project Manager

Upsilon Global, , Spain, España
Hace 14 días
Descripción del trabajo

Upsilon Global - Streamlining Clinical Trials

Freelance Clinical Project Manager - Homebased (EU) - Canadian sponsor - multiple studies

Upsilon Global are looking to speak to Clinical Project Managers with experience running European trials for North American / Canadian sponsors, on behalf of a small European CRO partner.

Our CRO partner has been awarded a portfolio of studies, varying in size, duration and budget, therefor we are particularly interested in speaking to CPMs who can demonstrate successes related to budgets and timelines.

You will be working closely with the Clinical Operations Director to ensure the launch, management and delivery of these studies is executed effectively, efficiently and in line with sponsor objectives, whilst also overseeing the patient experience and ensuring compliance and quality standards are maintained.

Key information

  • Position : Freelance CPM
  • FTE : 0.5-1.0 fte, depending on study
  • Indication : A range of studies / indications available
  • Start Date : December '25 / January '26
  • Location : Remote, EU

Key Responsibilities

  • Oversee all aspects of clinical trial execution, ensuring adherence to timelines, budgets, and quality standards.
  • Manage regulatory submissions and ethics committee documentation in line with French and EU requirements.
  • Monitor site activation, patient recruitment, and ongoing study progress, proactively addressing challenges.
  • Collaborate closely with sponsors, investigators, vendors, and regulatory authorities to ensure smooth study operations.
  • Identify study risks and implement effective mitigation strategies throughout the project lifecycle.
  • Provide leadership and guidance to clinical research teams, supporting training and performance.
  • Ensure compliance with ICH-GCP, local regulations, and gene therapy‑specific guidelines.
  • Requirements

  • Minimum 4 years of clinical trial project management experience.
  • Ability to demonstrate positive deliverables relating to study budgets and timelines essential.
  • In‑depth knowledge of EU clinical trial regulations and GCP guidelines.
  • Strong leadership, communication, and problem‑solving skills.
  • Fluency in English required.
  • For more details please apply using the link, or contact /

    Employment type

  • Contract
  • Job function

  • Science, Research, and Consulting
  • Industries

  • Biotechnology Research, Hospitals and Health Care, and Research Services
  • #J-18808-Ljbffr

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