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Job summary
A healthcare organization is seeking a Study Activations Project Coordinator to coordinate clinical research initiatives in Philadelphia. This role involves managing study start-up and related submissions, overseeing committee activities, and ensuring compliance with regulatory standards. Candidates should possess a Bachelor's Degree and relevant experience in project coordination, preferably in clinical research or oncology. The position offers a full-time employment opportunity with a mid-senior level responsibility.
Qualifications
Bachelor's Degree required; relevant education and experience may substitute.
5 years experience with computer programs, particularly Microsoft Suites.
1+ years experience coordinating Clinical Trial Management System activities.
Responsibilities
Coordinate study pipeline activities and TRACSS approval process.
Submit protocols and regulatory documents into CTMS.
Manage feasibility and review committee meetings and correspondence.
Skills
Coordination
Regulatory compliance
Data management
Meeting management
Education
Bachelor's Degree
Tools
Microsoft Office Suite
Clinical Trials Management System
Job description
A healthcare organization is seeking a Study Activations Project Coordinator to coordinate clinical research initiatives in Philadelphia. This role involves managing study start-up and related submissions, overseeing committee activities, and ensuring compliance with regulatory standards. Candidates should possess a Bachelor's Degree and relevant experience in project coordination, preferably in clinical research or oncology. The position offers a full-time employment opportunity with a mid-senior level responsibility.