Clinical Research Coord I

Job no: 514714
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Research/Scientific/Grants
Department:29050405 - MD-CARDIOLOGY-RESEARCH

Classification Title:

Clinical Research Coordinator I

Job Description:

Research
Attends cardiology clinics for the purpose of screening, recruiting, managing and evaluating investigational drugs and/or procedures including physical exams, Vitals, phlebotomy, interventional and non-interventional cardiac procedures/test and lab processing. Educates and motivates patients with regard to study compliancy goals. Knows appropriate study procedures for recruiting, managing of study patients and for reporting of side effects and un-blinding procedure. Visits any area of the hospital necessary for recruitment, evaluation or communication to other services in the interest of smoothly coordinating patient care before, during and after a patient participates in a research project. Develop study in-services for all medical personnel involved in a particular trial.

Communications
Initiates and organizes meetings as needed between investigators to discuss meshing various projects, the status of each in relation to others, and participates in problem solving discussions. Submits weekly reports to update sponsors, principal and co-investigators on the respective studies. Coordinates research facility utilization through communications with other research personnel and hospital services. Remains available during working hours, and on an on-call basis for recruiting, completing protocol procedures and for consultation on protocol related problems issues related to research projects.

Expected Salary:

$38,900 - $40,000

Minimum Requirements:

Associate's degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience.

Preferred Qualifications:

Skillful direction of professionals and non-professional to maintain excellent care while preserving protocol guidelines. Efficient collection and management of data. Knowledgeable of FDA regulations, methods, procedures, and ethics, related to research.

Special Instructions to Applicants:Upload CV for consideration for this position.

This is a time-limited position.

Application must be submitted by 11:55 p.m. (ET) of the posting end date.

Health Assessment Required:Yes

Advertised: 23 Sep 2020 Eastern Daylight Time
Applications close: 01 Oct 2020 Eastern Daylight Time