CLINICAL RESEARCH COORD A
Duties: The Clinical Research Coordinator A is responsible for data quality and documentation for assigned clinical trials conducted within the Division of Gynecologic Oncology to ensure that the clinical data collection and consequent data entry is accurate and all protocol requirements are captured. This position will also include responding to queries, interfacing with monitors, preparing for audits, screening/consenting subjects, scheduling and reviewing clinical assessments from research participants and assisting with regulatory responsibilities. Processing and shipping specimens will also be required.
Qualifications: BS degree and 1 to 3 years of experience; preferably in research, or an equivalent combination of education and experience required. Must be able to work flexible hours. Position requires highly motivated, articulate individual with excellent oral and written communication skills. The candidate should possess the ability to work independently and also as part of a team. Strong planning, organizational and prioritizing capabilities along with problem solving skills desired.
Reference Number: 40-30241
Salary Grade: 025
Employment Type: Exempt
Org: WM-Ctr for Res on Reprod and Women's Health
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