Supervisor, Clinical Research
Core
Oversee coordination and conduct of complex clinical trials, ensuring regulatory compliance and data integrity while leading research staff.
Role type
Senior IC clinical research supervisor
Builds
Clinical trial execution and operations management
Domain
Healthcare / Clinical Research
Required skills
Clinical trial management, Regulatory compliance (GCP, FDA, Common Rule), Data quality assurance, Team leadership, Project management, Protocol review
Preferred skills
Experience with CTMS and Document Management Systems, Audit preparation, Staff training and development
Technologies
CTMS, DHS, Microsoft Access, Excel, Case Report Forms (CRFs)
Responsibilities
Provide guidance and mentorship to clinical research coordinators; Oversee data management tasks and ensure data integrity; Conduct reviews of informed consent documents and eligibility criteria; Lead project meetings and coordinate interdepartmental research projects; Ensure adherence to Good Clinical Practice and institutional guidelines; Assist in developing training materials for research staff.
Seniority
Senior, hands-on IC