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 data integrity and compliance with Institutional Review Boards, FDA regulations, and 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
coordination of clinical research protocols
patient eligibility assessment for studies
informed consent process management
IRB submission and amendment handling
data integrity verification and analysis
compliance with FDA and federal regulations
Nice-to-have
experience in observational study design
manuscript writing and grant support
interdisciplinary team collaboration skills
internal and external quality review participation
Key Requirements
Bachelor's Degree in Biological Sciences or related field
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