CLINICAL RESEARCH COORD A
Duties: The Clinical Research Coordinator A will provide research support to the Department of General Internal Medicine. The coordinator will be responsible for all aspects of research project data collection, including maintaining the study website, participant recruitment, enrollment, study protocol implementation, data collection, and data entry. The research coordinator will also assist with project administration, including IRB management, adverse event reporting, and following up with participants for study milestones.
The Clinical Research Coordinator A will have active involvement in the planning and implementation of patient recruitment into studies and will also maintain a patient caseload once the patients are enrolled.
Qualifications: A Bachelor's Degree and 1 year to 3 years of experience or an equivalent combination of education and experience is required. Excellent communication, interpersonal and organizational skills. Understanding of regulatory compliance issues preferred. Experience working with electronic systems and data systems, and understanding good data management practices preferred. Ability to work effectively both independently and as part of a team. Familiarity with MS Office Suite is essential. Position contingent upon funding.
Reference Number: 40-29699
Salary Grade: 025
Employment Type: Exempt
Org: DM-General Internal Medicine
Job Family: I-Technical/Professional Research