The role involves coordinating and overseeing clinical research protocols investigating hematology malignancies primarily within observational studies
Job Summary
The role involves coordinating and overseeing clinical research protocols investigating hematology malignancies primarily within observational studies.
Candidates will be responsible for identifying patient eligibility, discussing studies with families, and obtaining informed consent.
The position requires ensuring compliance with Institutional Review Boards, FDA regulations, and maintaining strict data integrity.
Matching Summary
The role involves coordinating and overseeing clinical research protocols investigating hematology malignancies primarily within observational studies.
Skills & Requirements
Must-have
coordinate clinical research protocols
assess patient eligibility for studies
obtain informed consent from patients
ensure data integrity and collection
support IRB and FDA compliance
Nice-to-have
experience with observational studies
collaborate with interdisciplinary teams
participate in manuscript writing
prepare grant submissions
analyze and summarize research data
Key Requirements
Bachelor's Degree in Biological or Health Sciences