Senior Clinical Project Manager
Core
Lead cross-functional teams to oversee the execution of complex clinical trials for pharmaceutical, biotechnology, medical device, and consumer health clients, ensuring delivery per contractual commitments and regulatory guidelines.
Role type
Senior Clinical Project Manager (IC)
Builds
Clinical trials for pharma, biotech, medical device, and consumer health clients
Domain
Healthcare / Clinical Research / Contract Research Organization (CRO)
Required skills
Clinical trial management, CRO environment experience, Respiratory/rare disease study management, General medicine study management, Budget management, Team performance monitoring, Protocol and report preparation, SOP development, Regulatory compliance (GCP/ICH), Electronic data capture knowledge
Preferred skills
CRA experience, Nursing degree or relevant medical background, Microsoft Office proficiency
Technologies
Electronic data capture systems, Microsoft Office (Word, Excel, Outlook)
Responsibilities
Manage and coordinate assigned clinical projects; Manage project-specific services (central labs, drug shipments); Coordinate project team members and interact with Sponsors and Investigators; Collect and manage study data documentation; Monitor workload and team performance; Plan and monitor team tasks; Coordinate Clinical Research Associates and Clinical Monitors; Collaborate with Biometrics, Safety, and Regulatory teams; Assist in preparing protocols, CRFs, and Clinical Study Reports; Deliver project-specific trainings; Organize Monitor and Investigator meetings; Perform co-monitoring visits; Act as a tutor for junior project managers; Prepare SOPs for clinical research activities.
Seniority
Senior, hands-on IC