Clinical Trial Manager

Precision Medicine Group is hiring a Clinical Trial Manager in Hungary to take the operational lead on oncology studies and become the central point of coordination across multi-country clinical programs.

About the Role

As a Clinical Trial Manager based in Hungary, you will serve as the operational nucleus for the studies you oversee, directing Clinical Research Associates (CRAs) and steering every clinical dimension of your trials across several countries. The focus is on keeping work within scope, on schedule, and consistently high in quality. We're looking for a driven, detail-oriented professional who brings a consultative, partnership-minded approach to trial delivery and genuinely enjoys solving complex problems in a fast-moving setting.

Key Responsibilities

• Own the operational delivery of clinical activities throughout the trial lifecycle — site identification, start-up, enrollment, site support, monitoring strategy and execution, data cleaning, and close-out.
• Drive assigned studies to successful completion while ensuring all trial deliverables are met.
• Coordinate clear communication, regulatory documentation, and continuous trial oversight in partnership with cross-functional colleagues.
• Guide CRAs as they build site relationships covering monitoring, regulatory, IP, site payments, and overall site correspondence.
• Anticipate threats to timelines and deliverables, and propose inventive, decisive action plans for the team and sponsor.
• Mentor and train team members, keeping everyone aligned on study priorities to maximize client satisfaction.

Qualifications

• Bachelor's degree (or an equivalent mix of education and experience) in a science or health-related discipline, with oncology exposure.
• Proven experience leading the clinical elements of studies across multiple countries within a CRO, pharmaceutical, or biotech organization, in a dedicated clinical lead capacity.
• Substantial clinical trial management experience in oncology.
• Solid working knowledge of GCP/ICH guidelines and the clinical development process.
• Willingness to travel domestically and internationally, including overnight stays.
• Strong written and spoken English communication skills.
• Proficiency with MS Office, MS Project, and PowerPoint, plus clinical systems such as CTMS, eTMF, EDC, and IXRS.
• Command of medical terminology, ICH-GCP, and relevant regulatory guidance and SOPs.

About Precision Medicine Group

Precision Medicine Group is a precision-medicine CRO advancing oncology and rare disease research. By uniting innovative trial design, expert operational and medical teams, and advanced biomarker and data analytics, we connect specific mutations to targeted treatments and deliver insights that sharpen real-time development decisions. Precision Medicine Group is an Equal Opportunity Employer.

How to Apply

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