Clinical Research Coordinator -

Bayfrontstpete; Wesley Chapel (FL); On-site; USD 42,000 - 54,000; Full time

Job summary

Bayfrontstpete in Florida is seeking a Clinical Research Coordinator to support two Orthopedic FMC locations in Wesley Chapel and Tampa. The role involves coordinating research activities, screening patients for study eligibility, and assisting with study visits.

The majority of patient activity occurs at the Wesley Chapel location and requires solid clinical research knowledge. Responsibilities include administering quality-of-life questionnaires and collecting data for various clinical

Qualifications

• Bachelor’s degree in health-related field or equivalent; one year of clinical research or healthcare experience if using an associate degree; graduate of allied health program with one year of clinical experience.
• If no degree, experience substituted at two-for-one ratio with minimum one year clinical research experience.
• One year of healthcare experience required.
• RNs and other Clinical Research Coordinators involved in direct patient care may require licensure by medical director; BLS/Healthcare Provider certification required.

Responsibilities

• Screen patients for study eligibility.
• Assist with patient study visits and data collection.
• Administer quality-of-life questionnaires.
• Enter data into clinical research databases and ensure accuracy.

Skills

Clinical research knowledge

Screening patients

Data entry

Education

Bachelor's degree in health-related field

Associate degree in related field

Graduate of allied health program

Job description

Position Summary

Participate in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research.

This employee would support research activities at two Orthopedic FMC locations:

• FMC, 2352 Bruce B. Downs Blvd., Wesley Chapel, FL
• FMC, 14547 Bruce B. Downs Blvd., Suite C, Tampa, FL

The majority of patient activity occurs at the Wesley Chapel location. The individual will need sufficient clinical research knowledge to screen patients for study eligibility and assist with patient study visits, primarily administering quality-of-life questionnaires and collecting study-related data to enter in to various clinical research databases.

Qualifications

• Must meet one of the following:
• Bachelor’s degree in health-related field (i.e., Healthcare Administrative, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management); or
• Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section); or
• Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section).
• If no degree, experience may be substituted at a two for one ratio and a minimum of one-year clinical research experience required.
• One (1) year of healthcare experience required
• All RNs and other Clinical Research Coordinators involved in direct patient care may be required to be licensed by the medical director.
• BLS/Healthcare Provider certification required.