The role involves coordinating and overseeing clinical research protocols investigating hematology malignancies primarily in observational studies
Job Summary
The role involves coordinating and overseeing clinical research protocols investigating hematology malignancies primarily in observational studies.
Candidates must ensure all necessary data is collected, reported appropriately, and verified for integrity while maintaining compliance with IRB and FDA regulations.
The position requires collaboration with an interdisciplinary research team to develop study plans, case report forms, and prepare grant submissions.
Matching Summary
The role involves coordinating and overseeing clinical research protocols investigating hematology malignancies primarily in observational studies.
Skills & Requirements
Must-have
clinical research protocol coordination
patient eligibility assessment
informed consent acquisition
IRB submission management
data collection and integrity verification
regulatory compliance with FDA and IRB
Nice-to-have
manuscript writing experience
grant submission assistance
interdisciplinary team collaboration
quality review participation
Key Requirements
Bachelor's Degree in Biological Sciences or related field
1 year of relevant Clinical Research experience required