Senior Regional Clinical Research Associate
Corcept TherapeuticsFull Time
Senior (5 to 8 years)
Key technologies and capabilities for this role
Common questions about this position
The role involves both remote and onsite visits, including performing qualification, initiation, interim, and close-out visits both remotely and onsite.
This information is not specified in the job description.
The role requires strong knowledge of ICH GCP guidelines, FDA regulations, and SOPs, experience in site monitoring including remote and onsite visits, reviewing monitoring reports, and ensuring protocol compliance and data integrity.
The position involves close collaboration with internal teams including US and EU Clinical Monitoring departments and Project Managers, working with other CRAs to maintain consistency, and promoting a collaborative team atmosphere.
A strong candidate is highly motivated, independent, with leadership skills to provide guidance and oversight to the CRA team, experience in clinical trial monitoring, and the ability to ensure compliance with GCP, FDA regulations, and SOPs.
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