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 must ensure all necessary data is collected, reported appropriately, and verified to maintain strict data integrity standards.
The position requires supporting activities to ensure compliance with Institutional Review Boards, the FDA, and federal regulations.
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
obtain informed consent from patients
ensure IRB and FDA compliance
collect and verify clinical data
collaborate with interdisciplinary teams
Nice-to-have
experience in observational studies
manuscript writing capabilities
grant submission preparation skills
data analysis and reporting expertise
Key Requirements
Bachelor's Degree in Biological or Health Sciences
1 year of relevant Clinical Research experience required