Job Posting Title Clinical Research Coordinator

Bayfrontstpete; Tampa (FL); Hybrid; USD 52,000 - 70,000; Full time

Job summary

Bayfrontstpete seeks a Clinical Research Coordinator to participate in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials. The role supports research activities at two FMC locations: Wesley Chapel and Tampa, FL.

You will screen patients for study eligibility and assist with patient visits, primarily administering quality‑of‑life questionnaires and entering study data into databases.

Qualifications

• Must meet one of the following degree options or equivalent experience.
• One year of clinical research or healthcare experience required.
• One year healthcare experience; RN or other clinical research coordination roles may apply.
• BLS/Healthcare Provider certification required.

Responsibilities

• Participate in development, coordination and implementation of research and administrative strategies for clinical trials.
• Support research activities at FMC locations in Wesley Chapel and Tampa, FL.
• Screen patients for study eligibility, assist with visits, administer QoL questionnaires and enter data into databases.

Skills

Clinical research knowledge

Patient screening

Data collection

Education

Bachelor’s degree in health-related field

Associate degree in related field

Graduate of an accredited 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.