Clinical Research Coordinator must have 1 or more years experience in clinical research. The primary role is to coordinate phase II-IV clinical research for investigational new drug studies. Current trials include Diabetes, High Cholesterol, Renal Disease, Asthma, Low Testosterone and more. This is not a remote work position.

Responsibilities:

Involves in the patient screening and enrollment for the clinical studies Preparing and maintaining clinical trial source documents Conducting study visits, including vital signs, ECG, blood draw and processing Completing and ensuring the quality of case report forms Maintaining and dispensing drugs Preparing for site monitoring visits Preparing for site selection visits Maintaining documentation regarding all aspects of the study; Maintaining patient confidence and protects operations by keeping information confidential

Skills/Qualifications:

Must have 1 or more years of Research Coordinator experience. Bilingual preferred. Current CPR required, IATA certification preferred, GCP certification preferred. Medical Assistant or LPN preferred. Bachelor's Degree in a related field preferred. Good interpersonal and organizational skills. Demonstrated strong communication, leadership and presentation skills. Self-directed, proactive and timely in the management of the assignments. Clinical Research of South Nevada is an equal opportunity employer and a drug free and smoke free workplace.

Job Type:

Full-time Job Type:

Full-time Pay:

$15.00 - $25.00 per hour

Work Location:

In person