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, obtaining informed consent, and managing IRB submissions and modifications.
The position requires ensuring compliance with Institutional Review Boards, FDA regulations, and federal industry sponsor requirements.
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
manage IRB submissions and amendments
ensure data integrity and reporting
collaborate with interdisciplinary teams
Nice-to-have
experience in observational studies
manuscript writing capabilities
grant submission support experience
internal and external quality reviews
data analysis and query interpretation
Key Requirements
Bachelor's Degree in Biological or Health Sciences
1 year of relevant Clinical Research experience required
2-4 years of relevant experience preferred
Successful completion of background check
Drug screen or physical may be required post-offer