Job Overview
* Clinical Research Associate (CRA) I plays a pivotal role in ensuring the smooth execution of clinical trials.
Key Responsibilities Include:
Clinical Research and Compliance
* Evaluate site performance, providing recommendations for site-specific actions to maintain regulatory compliance.
* Conduct site qualification, site initiation, interim monitoring, site management, and close-out visits.
Required Skills and Qualifications:
* Demonstrate strong analytical skills to evaluate overall site performance.
* Excellent communication skills to provide recommendations and communicate serious issues to the project team.
Benefits:
* Award-winning organization recognized for its commitment to innovation and excellence.
* Opportunity to work with a diverse team of professionals passionate about advancing healthcare.
About the Role:
This is an exciting opportunity to join our dynamic team as a Clinical Research Associate (CRA) I. As a CRA I, you will be responsible for conducting site qualification, site initiation, interim monitoring, site management, and close-out visits. You will evaluate the overall performance of the site and its staff, providing recommendations for site-specific actions. Your excellent communication skills will enable you to effectively communicate serious issues to the project team. We are seeking a motivated individual who is passionate about clinical research and committed to delivering high-quality results.