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: A Bachelor's Degree and 1 to 3 years of experience or equivalent combination of education and experience required.

Reference Number: 40-27674

Salary Grade: 025

Employment Type: Exempt

Org: WM-Ctr for Res on Reprod and Women's Health

Special Requirements:

Job Family: I-Technical/Professional Research

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