Clinical Trial Manager
Core
Oversee critical clinical trial activities including site management, clinical monitoring, and central monitoring to ensure patient safety, data integrity, and regulatory compliance.
Role type
Senior Clinical Trial Manager
Builds
Global clinical research programs and complex trial portfolios
Domain
Healthcare / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | client delivery
Required skills
Clinical site management, Clinical monitoring, Central monitoring, Risk management, GCP/ICH guidelines, Budget management, Contractual considerations, Cross-functional team leadership, Inspection readiness, Clinical trial systems proficiency
Preferred skills
Risk-based monitoring, Clinical trial financial principles, Root cause analysis, Conflict resolution, Stakeholder management, Coaching and mentoring
Technologies
CTMS, EDC, eDiary, ePRO, TMF, IVRS/IWRS, Central monitoring platforms
Responsibilities
Provide oversight of site management, clinical monitoring, and central monitoring activities; Oversee site interactions from activation through closeout; Identify and mitigate critical data, process, and operational risks; Review study scope, budget, and protocol requirements; Coordinate with functions including Study Start Up, Patient Recruitment, Data Management, Medical Monitoring, Pharmacovigilance, and Quality Assurance; Develop and maintain clinical study tools and templates; Oversee CRA and Central Monitor resourcing and delivery quality; Monitor quality and progress of clinical deliverables; Support corrective and preventive actions and inspection readiness; Coach and mentor other Clinical Trial Managers.
Seniority
Senior, hands-on IC with mentorship responsibilities