CLINICAL RESEARCH COORD B
Duties: The Clinical Research Coordinator B (CRC B) will conduct the coordination of Phase I-IV clinical trials, as well as multi-center trials, working with partnering institutions on budgets, completing PRAs, and IRB documentation preparation. Studies are industry funded and/or federally funded investigator initiated trials. This position will provide supervision and training for lower level Research assistants (students, temporary workers) and Research coordinators. CRC B will be responsible for the coordination, organization and maintenance of all documentation required by Sponsor or CRO; resolve data queries with Sponsor or CRO; recruit, screen and enroll potential study subjects; participate in the conduct of audits; process and ship blood and specimens; schedule patient visits and any necessary testing; obtain records required to complete case report forms; conduct initiation, monitoring and closeout visits with Sponsor or CRO; create study budgets; work with limited supervision in the management
of clinical trials and use independent judgment.
Qualifications: A Bachelor's Degree and 2 years to 4 years of experience or equivalent combination of education and experience required.
Reference Number: 40-28499
Salary Grade: 026
Employment Type: Exempt
Org: DM-Cardiovascular Medicine
Job Family: I-Technical/Professional Research