Oncology Clinical Protocol Coordinator
Sarah Cannon Research Institute
60K–80K a year
Behavioral Health Market Context
Apply Nowvia Learn4Good
Job Description
ns related to clinical trials. This role is part of a mission-driven team dedicated to advancing cancer treatments for patients across the globe.
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Qualifications
- •Candidates should have extensive oncology knowledge, experience with Clinical Trial Management Systems, and an Associate’s Degree
Benefits
Responsibilities
- •A leading oncology research organization is seeking a Research Protocol Coordinator to assist with initiatives within the Research Protocol Operations department
- •Responsibilities include monitoring processes, managing tracking activities, and assisting in communications related to clinical trials
- •This role is part of a mission-driven team dedicated to advancing cancer treatments for patients across the globe
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