Job Summary: Coordinate various research trials for the Institute for Global Health, including early or 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 3 years related experience or equivalent combination of education and experience, experience with clinical research protocols, knowledge of medical terminology, computer skills, and good written/oral communication and organizational skills required.

Preferred Qualifications:

SOCRA or ACRP certification preferred.

Work Days:

Monday - Friday, Days with occasional weekends

Message to Applicants:

Recruitment Office: Human Resources