Clinical Trial Manager

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Occupation tasks (O*NET)

Public-domain labor data — prepare examples for 2–3 of these.

• Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
• Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
• Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
• Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
• Inform patients or caregivers about study aspects and outcomes to be expected.
• Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
• Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
• Oversee subject enrollment to ensure that informed consent is properly obtained and documented.

O*NET source

Company facts (cached)

Website: precisionmedicine.com

Public cache only — not an employee review.

Role overview (listing rewrite)

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…

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Questions to ask them

• What does success look like in the first 90 days for this role?
• How is the team structured, and who would I work with most?
• What tools and systems does this role use daily?
• Is the work primarily based in Hungary, hybrid, or fully remote?