Clinical Research Coordinator - Blood Cancer & BMT Trials
Sarah Cannon Research Institute
Behavioral Health Market Context
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Job Description
intaining regulatory documents, and communicating progress to management. Strong skills in medical terminology, project management, and public presentation are required.
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Qualifications
- •Candidates should have at least one year of oncology experience and an Associate’s or Bachelor’s degree
- •Strong skills in medical terminology, project management, and public presentation are required
Benefits
Responsibilities
- •A clinical research organization in Florida seeks a Clinical Research Coordinator to manage patient enrollment in blood cancer clinical trials
- •Responsibilities include ensuring patient safety, data integrity, and compliance with study protocols
- •The role involves coordinating site meetings, maintaining regulatory documents, and communicating progress to management
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