Clinical Research Coord II

Location
Main Campus (Gainesville, FL)
Posted
Jan 13, 2021
Employment Type
Full Time
Institution Type
Four-Year Institution

Job no: 515474
Work type: Staff Full-Time
Location: Main Campus (Gainesville, FL)
Categories: Research/Scientific/Grants
Department:29050700 - MD-ENDOCRINOLOGY

Advertised: 12 Jan 2021 Eastern Standard Time
Applications close: 26 Jan 2021 Eastern Standard Time

Classification Title:

Clinical Research Coordinator II

Job Description:

The Department of Medicine, Division of Endocrinology, Diabetes & Metabolism is looking to fill a Clinical Research Coordinator II position. The Clinical Research Coordinator will maintain IRB approval for each on-going clinical trial, recruit and enroll subjects in on-going clinical trials, coordinate history and physicals on clinical trial subjects, assist with continuing care of those subjects as well as maintain all regulatory and sponsor required documentation. The duties for this position include but not limited to:

A. Prepares reports to IRB (Institutional Review Board) of any changes in protocol or adverse events. Reviews protocols at least yearly and provide needed documentation to IRB and Clinical Translational Sciences Institute (CTSI).

B. Recruits and enters eligible candidates in the study after explanation of purpose, benefits and risks of the project to them, obtains an informed consent as required in the protocol.

C. Coordinates a complete history and physical examination and obtains appropriate urine and blood samples as described in the protocol.

D. Coordinates administration of drugs and prescriptions to patients on the study when necessary.

E. Collects and maintains all records related to each patient. The project statistician will use this data to analyze the results for the project.

F. Arranges follow-up visits for each patient. This includes an appointment card, and a phone reminder the day prior to the scheduled visit.

G. Arranges for payment per protocol, if indicated, of each subject who participates in this study.

H. Maintains adequate inventory of supplies to carryout the procedures indicated in the protocol.

I. Maintains regular contact and follow-up with key persons in various laboratories involved in the protocol in order to confirm samples are being received and processed.

J. Performs other duties as may be necessary to conduct study and carryout related functions of the Division.

Expected Salary:

$44,700 - $48,000

Minimum Requirements:

Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.

Preferred Qualifications:

LPN or RN and two years of appropriate experience.
• Ability to draw blood and take vitals for research patients
• A working knowledge of NIH and UF policies and procedures for research accounts
• Strong written and oral communication skills

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

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