Job Summary
The Clinical Research Coordinator is tasked with overseeing the clinical process involving research participants. This role necessitates adherence to established study protocols, conducting various tests, and gathering essential data throughout the research process.
Responsibilities
- Ensure compliance with study protocols and procedures during research.
- Perform tests and collect relevant data from research participants.
- Maintain precise documentation through case report forms.
- Manage the inventory of study supplies efficiently.
- Address and report any regulatory issues to the Institutional Review Board.
Qualifications
- Bachelor’s degree in a related discipline, with a preference for science fields.
- A minimum of 4 years of clinical experience is essential, particularly within a research environment.
- Familiarity with FDA regulatory standards and requirements is necessary.
