CLINICAL RESEARCH COORD B
Duties: Support ongoing clinical trials in medical and head and neck oncology by consenting patients, maintaining databases, completing adverse events reporting to regulatory authorities and industry sponsors. Responsible for extraction of data from clinical records, coordination or research related testing and sample processing with the patient and rest
of the research staff. Entry of all data in a timely fashion into both university and industry databases. Will help develop and work with study budgets to coordinate accurate billing for patient research activities. Will be completely responsible for overseeing successful execution of research projects assigned. Will accurately extract data from databases in form usable for manuscript or other type of publication. Will be responsible for all regulatory filings required for maintaining active status of the trial with the IRB, the Clinical Trials Scientific Committee and Data Safety Monitoring Committees, and be able to work effectively with study monitors and auditors on an as needed basis.
Must be a team player, experience with handling research blood samples preferred but not required.
Qualifications: The minimum of a Bachelor's degree and 2 years to 4 years of experience or equivalent combination of education and experience required.
Reference Number: 40-26232
Salary Grade: 026
Employment Type: Exempt
Job Family: I-Technical/Professional Research