Oncology Clinical Project Lead - Remote (Spain)

Precision Medicine Group

Madrid

Remote

EUR 90,000 - 130,000

Full time

5 hours ago
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Job summary

Precision for Medicine Group is seeking a Senior Clinical Project Manager (Oncology) to oversee full-service clinical trials from negotiation to delivery. The role supports international studies, budgets, timelines, and client relationships, with a focus on high-quality operational execution.

You will lead cross-functional teams, coordinate with sponsors, and drive study protocols and documentation while ensuring GCP compliance.

Qualifications

  • Degree or similar life science qualification or equivalent experience.
  • Prev. full-service/global PM role in CRO essential.
  • At least 4 years full-service PM in clinical trials (CRO).
  • Experience managing oncology studies.
  • Working understanding of GCP/ICH guidelines and clinical development process.
  • Ability to travel domestically and internationally.
  • Proficient in English (written and spoken).
  • Strong computer skills: MS Office, MS Project, PowerPoint; software: CTMS, eTMF, EDC, IXRS.

Responsibilities

  • Lead clinical projects across global/regional (Ph I–IV) trials within Oncology.
  • Serve as primary client contact for proposal activities and presentations.
  • Coordinate with project team and senior management from Precision and sponsors.
  • Oversee all aspects of a clinical trial or trials; total project management across data management, safety, clinical, medical monitoring, biostatistics.
  • Prepare project status updates and define deliverables and success metrics.
  • Contribute to study protocols and other study documentation (plans, informed consents, site contracts, budgets).

Job description

Precision for Medicine Group is seeking a Senior Clinical Project Manager (Oncology) to oversee full-service clinical trials from negotiation to delivery. The role supports international studies, budgets, timelines, and client relationships, with a focus on high-quality operational execution.

You will lead cross-functional teams, coordinate with sponsors, and drive study protocols and documentation while ensuring GCP compliance.

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