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IQVIA
Overview
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
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Compensation
$71,900 - $169,300 / YEAR
Posted
9 days ago
The Senior CRA is responsible for monitoring and managing clinical sites to ensure strict adherence to study protocols, regulatory requirements, and sponsor expectations. They will conduct various site visits, facilitate subject recruitment, and maintain essential study documentation to ensure high-quality clinical research data.
$87,200 - $169,300 / YEAR
1 month ago
The Study Start-Up CRA is responsible for managing site selection, study-specific start-up activities, and ensuring deliverables are met for Phase I-IV trials. They act as the primary contact for trial sites, facilitating document collection, regulatory submissions, and site greenlight processes.
$71,900 - $145,300 / YEAR
2 months ago
TriHealth
The coordinator manages all components for successful clinical research trials, functioning as an educator, consultant, and liaison while ensuring safety, integrity, and efficiency by applying knowledge of good clinical practices. This involves coordinating Phase II through IV trials from initial sponsor contact through study completion and close-out, including marketing and determining protocol feasibility.
Salary not listed
Rovia Clinical Research
This role involves managing the day-to-day operations of clinical studies, ensuring execution aligns with protocols, GCP, and SOPs, including coordinating startup activities, overseeing facility issues, and leading site meetings. Responsibilities also include monitoring enrollment progress, ensuring timely data entry into platforms like EDC, leading study visits, and providing guidance and training to site research staff.
$55,000 - $70,000 / YEAR
3 months ago
