Coordinate and oversee clinical research protocols investigating hematology malignancies, primarily in observational studies
Job Summary
Coordinate and oversee clinical research protocols investigating hematology malignancies, primarily in observational studies.
Ensure all necessary data is collected, reported, and verified for integrity, while supporting regulatory compliance with IRB, FDA, and industry sponsor regulations.
Collaborate with an interdisciplinary research team and participate in manuscript writing and grant submissions.
Matching Summary
Coordinate and oversee clinical research protocols investigating hematology malignancies, primarily in observational studies.
Skills & Requirements
Must-have
clinical research protocols
hematology malignancies
patient eligibility assessment
informed consent
IRB submissions
data collection and reporting
regulatory compliance
Nice-to-have
interdisciplinary research team collaboration
manuscript writing
grant preparation
quality assurance reviews
Key Requirements
Bachelor's Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience