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Syneos Health

Senior Clinical Trial Manager

Syneos Health

. Provide site management oversight, clinical monitoring, and central monitoring deliverables .

Posted 10/6/2026full-timeMelbourne • AustraliaSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

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 maintain data integrity and patient safety throughout the clinical trial process.

Highest-signal resume keywords
Clinical Site ManagementGood Clinical Practice ComplianceRisk-Based MonitoringBudget ManagementTeam Leadership

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical MonitoringProtocol ReviewData IntegrityRisk AssessmentClinical Trial ManagementStudy Start Up CoordinationClinical Monitoring Plans DevelopmentUAT OversightAudit Trail ReviewConflict Resolution
Soft Skills
Critical ThinkingProblem-SolvingTeam AlignmentCommunicationCoaching
Tools & Technologies
CTMSEDCEDiaryEPROsTMFIVRS/IWRSDashboards
Industry Keywords
Clinical TrialsRegulatory ComplianceInternational EnvironmentPatient SafetyInvestigator Payments

About the role

Key responsibilities & impact
  • Provide site management oversight, clinical monitoring, and central monitoring deliverables
  • Focus on patient safety, protocol/GCP/regulatory compliance, and data integrity
  • Oversee site interactions from activation through closeout, including recruitment and investigator payments where applicable
  • Review study scope, budget, protocol content, contractual obligations, and clinical project team awareness
  • Identify, escalate, and mitigate risks affecting timelines, quality, budget, and protocol execution
  • Participate in and present at key meetings, including Kick Off Meetings
  • Serve as an escalation point for investigator site staff and principal investigators
  • Coordinate with Study Start Up, Patient Recruitment, Data Management, and other functional leaders
  • Develop and maintain clinical study tools and templates, including Clinical Monitoring Plans
  • Ensure CTMS, dashboards, and other systems are configured and available; oversee UAT and audit trail reviews
  • Coordinate study-team training on protocols, CRFs, dashboards, SOPs, plans, guidelines, data plans, and timelines
  • Oversee CRA and Central Monitor resourcing, assignments, conduct, compliance, and delivery quality
  • Review oversight dashboards and clinical trial systems including CTMS, EDC, eDiary, ePROs, TMF, IVRS/IWRS, and central monitoring dashboards
  • Oversee monitoring strategy compliance and participate in risk assessment planning
  • Review site and central monitoring documentation and ensure timely revisions, approvals, and delivery
  • Provide status updates and solutions to clients, project management, and leadership
  • Support inspection readiness for clinical trial management
  • Oversee CRAs and Central Monitors, develop and support corrective action plans, and support data cut and lock deadlines
  • Provide staff performance feedback to line managers
  • Coordinate clinical activities across portfolios and coach or mentor CTMs when assigned

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
  • Strong conflict resolution skills
  • Ability to apply problem-solving techniques to resolve complex issues and apply a risk management approach
  • Critical thinking to determine causes and appropriate solutions when identifying issues
  • Moderate travel capability, approximately 20%

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition
  • Total rewards program
  • Total Self culture supporting authenticity and inclusion
  • Diversity, belonging, and inclusive workplace culture