Clinical Project Manager

50989
  • Paris, United Kingdom
  • Contract

Freelance Clinical Project Manager – 12-Month Contract

We are seeking an experienced Clinical Project Manager to support the delivery of early-phase clinical trials for an innovative, early-stage biotech organization. This is a 12-month freelance contract, offering the opportunity to make a tangible impact in a fast-paced, hands-on clinical operations environment.

Role Overview:
The Clinical Project Manager will oversee the operational delivery of Phase II clinical trials, working closely with internal teams, CRO partners, and investigative sites. The role also involves mentoring junior clinical staff and contributing to the development of clinical operations processes as the organization grows.

Key Responsibilities:

  • Lead day-to-day operational management of Phase II clinical trials.

  • Oversee CROs, vendors, and site relationships to ensure timely and high-quality study delivery.

  • Manage study timelines, milestones, and deliverables.

  • Identify operational risks and implement mitigation strategies.

  • Ensure compliance with ICH-GCP, regulatory requirements, and internal SOPs.

  • Support preparation and maintenance of study documentation and trial plans.

  • Mentor and support Clinical Trial Assistants (CTAs) or junior clinical team members.

  • Collaborate cross-functionally with clinical development, regulatory, safety, and data management teams.

Required Experience & Skills:

  • Minimum of 3 years’ experience in clinical management within biotech or pharmaceutical organizations.

  • Strong understanding of clinical operations and ICH-GCP guidelines.

  • Proven experience supporting or mentoring junior clinical team members (e.g., CTAs).

  • Demonstrated ability to manage CROs and vendors effectively.

  • Comfortable working in an early-stage biotech environment with a hands-on approach.

  • Adaptable, collaborative, and solutions-focused.

Additional Details:

  • Hybrid working arrangement available, flexible on a weekly or bi-weekly basis.

  • Must be authorized to work in the United Kingdom and able to commute to the office location.

This contract role is ideal for an experienced clinical operations professional who thrives in a dynamic, fast-moving environment and wants to play a key role in advancing early-phase clinical research.

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