Clinical Trial Manager

Precision Medicine Group

. Manage and operationally deliver clinical elements within trials, including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning, and close-out .

Posted 9/30/2026full-timeRemote • Serbia, Hungary, Poland, Romania, SlovakiaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials, including site selection, enrollment management, and regulatory compliance, with a strong focus on oncology. Proven ability to lead cross-functional teams and mentor team members while ensuring effective communication and oversight across multiple countries.

Highest-signal resume keywords

Clinical Trial ManagementOncology ExperienceGCP/ICH Guidelines MasteryCTMS Software ProficiencyCross-Functional Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementOncology ExperienceGCP/ICH GuidelinesMedical TerminologyData CleaningMonitoring PlanningRegulatory DocumentationEnrollment ManagementSite EngagementTrial Deliverables Execution

Soft Skills

Effective CommunicationMentoringProblem-SolvingRelationship BuildingTeam Collaboration

Tools & Technologies

MS OfficeMS ProjectPowerPointCTMSETMFEDCIXRS

Industry Keywords

Clinical DevelopmentCROPharmaBiotechRegulatory Guidance

About the role

Key responsibilities & impact

Manage and operationally deliver clinical elements within trials, including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning, and close-out
Execute assigned trials successfully and ensure completion of trial deliverables
Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trials
Collaborate closely with cross-functional team members
Mentor and train team members
Identify challenges to study timelines and deliverables and provide creative action plans to the team and sponsor
Lead CRAs in site relationships and oversight of monitoring, regulatory, IP, site payment, and site correspondence activities
Maintain focus on study priorities through cross-functional partnerships and effective communication
Serve as the central intelligence hub for managed studies and oversee clinical aspects across multiple countries

Requirements

What you’ll need

Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in oncology
Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, Pharma, or Biotech company in a dedicated clinical lead role
Significant clinical trial management experience in oncology
Working knowledge of GCP/ICH guidelines and the clinical development process
Availability for domestic and international travel, including overnight stays
Must be able to communicate effectively in English
Demonstrated computer skills with MS Office, MS Project, and PowerPoint
Software experience with CTMS, eTMF, EDC, and IXRS
Demonstrated ability to develop positive working relationships with internal and external organizations
Core understanding of medical terminology and clinical trial activities related to clinical development plan execution
Mastery of ICH-GCP, relevant Precision SOPs, and regulatory guidance
Candidates must be legally authorized to work in the country of employment without employer sponsorship

Benefits

Comp & perks

Remote work option
Mentoring and training of team members
Equal Opportunity Employer
Reasonable accommodation available during the application process