Responsible for the coordination and oversight of clinical research protocols investigating hematology malignancies primarily in observational studies
Job Summary
Responsible for the coordination and oversight of clinical research protocols investigating hematology malignancies primarily in observational studies.
Collaborates with an interdisciplinary research team and ensures that all necessary data is collected and reported as appropriate.
Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA, federal, state and industry sponsor regulations.
Matching Summary
Responsible for the coordination and oversight of clinical research protocols investigating hematology malignancies primarily in observational studies.
Skills & Requirements
Must-have
Clinical research protocols
Patient eligibility assessment
Informed consent process
IRB submissions and modifications
Data collection and reporting
Regulatory compliance
Nice-to-have
Manuscript writing
Grant submission preparation
Data analysis and interpretation
Interdisciplinary collaboration
Key Requirements
Bachelor's Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience