Clinical Trial Manager - Oncology

About the role

Precision for Medicine, a precision medicine CRO, is looking for an experienced Clinical Trial Manager to join its growing team. The role acts as the central hub for the studies managed, leading CRAs and overseeing all clinical aspects across multiple countries while ensuring timeline adherence, scope and quality delivery. Remote work is available in Hungary, Poland, Romania, Serbia, Slovakia, the UK or Spain.

Key responsibilities

• Manage and deliver the clinical elements of trials, including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning and close-out.
• Ensure assigned trials are completed successfully and that deliverables are met.
• Maintain clear communication, regulatory documentation and oversight of trials in close collaboration with other functional teams.
• Train and mentor team members and propose creative action plans for study timeline and deliverable challenges.
• Lead CRAs in building relationships with sites for high-quality oversight of monitoring, regulatory, IP, site payments and site correspondence.

Required profile

• Bachelor's degree or equivalent in a science or health-related field, including oncology experience.
• Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharma or biotech company (dedicated clinical lead role).
• Significant clinical trial management experience in oncology; CAR-T and radiopharmaceuticals experience is a strong plus.
• Working knowledge of GCP/ICH guidelines and the clinical development process.
• Availability for domestic and international travel, including overnight stays.
• Effective English communication; candidates must be legally authorised to work in the country of employment.

Required skills

• Computer skills: MS Office, MS Project, PowerPoint.
• Software experience: CTMS, eTMF, EDC, IXRS.
• Core understanding of medical terminology and clinical trial activities.