Global Oncology Project Manager - Europe (Remote)

Worldwide

United Kingdom

Remote

GBP 75,000 - 110,000

Full time

3 days ago
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Job summary

Worldwide Clinical Trials is seeking a Senior / Project Manager focused on Oncology in Europe, delivering Phase I-IV studies across global teams. This remote role requires strong leadership of cross-functional groups, stakeholder management, and adherence to ICH-GCP guidelines.

You will own start-up through closeout, manage budgets, drive risk mitigation, and partner with clients to ensure high-quality trials that meet timelines and regulatory standards.

Qualifications

  • University degree in Life Sciences or related field; 5+ years in clinical pharma.
  • Proven Oncology clinical project management experience.
  • Leadership of multidisciplinary teams; strong PM skills.
  • Financial acumen; manage project budgets and timelines.
  • ICH-GCP knowledge and regulatory awareness; English required.

Responsibilities

  • Lead the delivery of Phase I-IV trials from start-up to closeout.
  • Direct cross-functional teams, clients, vendors and subcontractors.
  • Develop and maintain project plans, timelines, and resources.
  • Manage budgets and ensure alignment with contracts and goals.
  • Serve as primary client contact to ensure satisfaction.
  • Identify risks and implement solutions to keep studies on track.

Skills

Oncology clinical project management
Stakeholder management
Cross-functional leadership
Budget management
ICH-GCP knowledge

Education

University degree in Life Sciences or related field

Tools

Project management software

Job description

Worldwide Clinical Trials is seeking a Senior / Project Manager focused on Oncology in Europe, delivering Phase I-IV studies across global teams. This remote role requires strong leadership of cross-functional groups, stakeholder management, and adherence to ICH-GCP guidelines.

You will own start-up through closeout, manage budgets, drive risk mitigation, and partner with clients to ensure high-quality trials that meet timelines and regulatory standards.

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