Clinical Trial Manager

Precision Medicine Group

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

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

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials, including site selection, monitoring, and regulatory compliance, with a strong focus on oncology. Proven ability to lead cross-functional teams and maintain effective communication to ensure successful trial execution across multiple countries.

Highest-signal resume keywords

Clinical Trial ManagementOncology ExperienceGCP/ICH Guidelines KnowledgeCTMS Software ProficiencyTeam Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementOncology ExperienceGCP KnowledgeICH Guidelines KnowledgeMedical TerminologyData CleaningMonitoring PlanningRegulatory DocumentationTrial ExecutionEnrolment Management

Soft Skills

Effective CommunicationMentoringRelationship BuildingProblem SolvingTeam Collaboration

Tools & Technologies

MS OfficeMS ProjectPowerPointCTMSETMFEDCIXRS

Industry Keywords

Clinical DevelopmentCROPharmaBiotechClinical Lead Role

About the role

Key responsibilities & impact

Manage and operationally deliver clinical elements within trials, including site selection, start-up, enrolment 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 in collaboration with functional team members
Mentor and train team members
Identify challenges to study timelines and deliverables and develop creative action plans for the team and sponsor
Lead CRAs in establishing site relationships and overseeing monitoring, regulatory, IP, site payment, and site correspondence activities
Maintain team focus on study priorities through cross-functional partnerships and effective communication to achieve client satisfaction
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 the field of 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 the English language
Demonstrated computer skills in 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 execution of a clinical development plan
Mastery knowledge of ICH-GCP, relevant Precision SOPs, and regulatory guidance, with ability to implement
Candidates must be legally authorized to work in the country of employment without employer sponsorship

Benefits

Comp & perks

Remote work arrangement
Career growth support and continued professional development
Mentoring and training opportunities
Domestic and international travel opportunities