Role OverviewThe Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines.
What You Will Do
Conduct various types of monitoring visits, including site selection, initiation, routine monitoring, and close-out visits, to evaluate the quality and integrity of site practices. Verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary.
Why It Might Be a Fit
A central part of this role involves building and maintaining strong communication with investigative sites. You will provide protocol training, set expectations, address site-level challenges, and support recruitment planning to help sites meet enrollment targets.
Requirements
- Bachelor's degree required; a scientific or healthcare discipline is preferred.
- 6 months –2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered.
- Basic knowledge of clinical research regulations (GCP/ICH).
- Ability to travel as required by the project.
Benefits
- Potential base pay range: $71,900.00 - $119,900.00
- Incentive plans, bonuses, and/or other forms of compensation may be offered
- Range of health and welfare and/or other benefits
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