Clinical Trial Manager

Syneos Health

. Provide site management oversight, clinical monitoring and central monitoring deliverables focused on patient safety, protocol/GCP/regulatory compliance and data integrity .

Posted 10/15/2026full-timeAthens • GreeceMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical site management and monitoring, ensuring compliance with Good Clinical Practice and regulatory requirements while effectively leading teams to achieve project milestones. Proficient in risk management and problem-solving techniques to address complex issues in clinical trial management.

Highest-signal resume keywords

Site ManagementClinical MonitoringRisk-Based MonitoringGood Clinical PracticeBudget Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementData IntegrityProtocol ComplianceRisk ManagementClinical Monitoring Plan Development

Soft Skills

Communication SkillsConflict ResolutionCritical ThinkingInterpersonal SkillsPresentation Skills

Tools & Technologies

CTMSEDCEDiaryEPROTMFIVRS/IWRS

Industry Keywords

Good Clinical PracticeICH GuidelinesRegulatory ComplianceClinical Study ToolsInternational Environment

About the role

Key responsibilities & impact

Provide site management oversight, clinical monitoring and central monitoring deliverables focused on patient safety, protocol/GCP/regulatory compliance and data integrity
Oversee site interactions from post-activation through site closeout, including recruitment and investigator payments
Identify critical data, process and protocol execution risks and implement mitigations
Review study scope, budget, protocol content and contractual obligations with the clinical project team
Identify and escalate risks to timelines, quality, budget and contracted scope
Participate in and present at key meetings, including Kick Off Meetings
Serve as an escalation point for investigator site communications and interact with principal investigators and site staff
Coordinate with Study Start Up, Patient Recruitment and Data Management to meet study milestones
Develop and maintain clinical study tools and templates, including the Clinical Monitoring Plan
Ensure CTMS, dashboards and other systems are configured, available and subject to required UAT and audit-trail reviews
Coordinate initial and ongoing study-team training
Oversee CRA and Central Monitor resourcing, site assignments, conduct and delivery risks
Ensure quality and visibility of clinical monitoring, central monitoring and site management deliverables
Review dashboards and clinical trial systems including CTMS, EDC, eDiary, ePRO, TMF, IVRS/IWRS and central monitoring dashboards
Ensure team compliance with monitoring strategy, CMP/SMP and risk plans
Review site and central monitoring documentation for quality, accuracy and regulatory risks
Interact with clients, project management, leadership and functional departments; provide status updates and solutions
Support inspection readiness for clinical trial management scope
Oversee CRAs and Central Monitors, assess compliance, support corrective action plans and meet data cut and lock deadlines
Provide performance feedback to line managers
May be assigned to larger, more complex trials

Requirements

What you’ll need

Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
Demonstrated ability to lead and align teams in the achievement of project milestones
Demonstrated capability of working in an international environment
Demonstrated expertise in site management and monitoring (clinical or central)
Preferred experience with risk-based monitoring
Understanding of clinical trial management financial principles and budget management
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
Good computer skills
Good communication, presentation and interpersonal skills
Strong conflict resolution skills
Ability to apply problem-solving techniques to resolve complex issues and apply a risk management approach
Critical-thinking ability to identify issues and determine appropriate solutions
Moderate travel may be required, approximately 20%

Benefits

Comp & perks

Career development and progression
Supportive and engaged line management
Technical and therapeutic area training
Peer recognition
Total rewards program
Inclusive culture
Reasonable accommodations when appropriate