Job Summary: Coordinate multiple research trials for the Institute for Global Health, including early to late phase FDA-regulated trials, and ensure compliance with federal guidelines. Interact and correspond with clinicians, sponsors, cooperative groups, Upstate's Institutional Review Board and regulatory agencies. Enroll, register and screen patients for clinical research trials; collect and submit clinical trial patient data. Perform various administrative duties, which may include proper collection and shipment of lab samples; billing support; maintenance of clinical research study supplies and drug accountability. Minimum Qualifications: Bachelor's degree and two years of relevant experience or equivalent combination of education and experience required. Experience with clinical research protocols, knowledge of medical terminology, computer skills, good written/oral communication and organizational skills required. Ability to work as a team member on behalf of more than one investigator. Preferred Qualifications: Experience with patient recruitment and enrollment preferred. SOCRA CCRP (Certified Clinical Research Professional) or willingness to participate in training toward certification preferred Work Days: M-F days with occasional evenings or weekends Message to Applicants: Recruitment Office: Human Resources