CLINICAL RESEARCH COORD A
Duties: The clinical research coordinator will be responsible for data entry, organizing, maintaining and assuring the accuracy of all study documentation. The coordinator will oversee one (1) or more clinical trials ensuring that the integrity of the protocol is maintained, timely completion of case report forms (CRFs and eCRFs), and ensures appropriate AEs and SAEs are reported to the sponsor and IRB per protocol. The CRC will participate in research clinic to explain the trial to the patient and family, screen and determine eligibility, consent and enroll patients, and complete any follow-up or research activity required. The CRC will conduct phone interviews if necessary. The CRC must complete relevant training to function in the role including electronic databases, processing and shipping specimens and phlebotomy. The CRC must be sufficiently knowledgeable about Microsoft word, Excel and other standard programs. The CRC must maintain professionalism and follow the guidelines of the institution.
Position is contingent on continued funding.
Qualifications: A Bachelor's Degree and 1 to 2 years of experience or equivalent combination of education and experience required.
Reference Number: 40-26802
Salary Grade: 025
Employment Type: Exempt
Org: SU-Surgery Administration
Special Requirements: Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.
Job Family: I-Technical/Professional Research