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The US Oncology Network
Overview
Responsible for managing research regulatory and administrative activities for clinical trials, including site qualification and document management. Collaborates with investigators and central operations to ensure compliance with SOPs, GCP, and federal regulations.
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Compensation
Salary not listed
Posted
24 days ago
Children's Healthcare of Atlanta
The Research Pharmacist manages investigational pharmaceutical care by evaluating and implementing research drug protocols. Responsibilities include the procurement, storage, and dispensing of study medications while ensuring compliance with state and federal regulations.
29 days ago
CHOC
The Clinical Research Coordinator II provides coordinator support for multiple human subjects' clinical research projects, performing all core CRC responsibilities with minimal supervision. This includes assessing protocol feasibility, preparing IRB submissions, identifying participants, coordinating data collection, maintaining accurate study records, and managing supplies.
$31 - $51 / HOUR
1 month 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.
2 months ago
