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Clinical Project Manager / Senior Clinical Project Manager - Clinical Trial Services

Precision Medicine Group
Remote, Hungary
Remote

About this role

About the Role

We are seeking a Clinical Project Manager / Senior Clinical Project Manager with oncology experience to lead full service global trials within Oncology. This role provides full-service oversight for clinical projects across global/regional Ph I-IV trials, managing client relationships, budgets, timelines, and cross-functional study teams. What You'll Do

  • Independently lead clinical projects in accordance with study budget and scope of work.

  • Serve as the primary client liaison, including participation in proposal activities and client presentations.

  • Liaise with the Project Team and senior management (including sponsor and Precision leadership) to drive study delivery.

  • Manage all aspects of a clinical trial or trials (data management, safety, clinical, medical monitoring, biostatistics, etc.).

  • Prepare project status updates for clients and management; identify deliverables, milestones and KPIs; escalate issues as needed.

  • Be an active member of the Project Team to optimize trial execution and efficiency.

  • Prepare and review study documentation (protocols, project plans, informed consents, site contracts, budgets).

  • Travel domestically and internationally as required. What We're Looking For

  • Degree or life sciences qualification, or equivalent.

  • Experience in a full-service/global Projekt Management role in CROs.

  • Extensive experience in Clinical Operations within a CRO and at least 4 years in full-service PM in a clinical trial setting.

  • Experience managing oncology studies.

  • Strong understanding of GCP/ICH guidelines and the clinical development process.

  • Ability to travel domestically and internationally including overnights.

  • Excellent English communication (written and spoken).

  • Strong presentation skills.

  • Proficiency with MS Office, MS Project, PowerPoint and software (CTMS, eTMF, EDC, IXRS).

  • Demonstrated ability to build positive working relationships with individuals and teams.

  • Solid understanding of medical terminology and clinical trial activities as they relate to the clinical development plan. Compensation & Benefits

  • The posting describes a high-energy, dedicated, collaborative environment with a focus on team development and work-life balance. Specific salary and benefits were not listed in the posting.

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