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Clinical Research Coordinator

  • LocationHialeah, FL 33012 - United States
  • Work TypeFull time
  • Positions1 Position
  • Published At:2 months ago
  • Job no: 41378
  • Category: Clinical

Job Description

A brilliant opportunity exists for an outstanding individual capable of fitting into this very rewarding Clinical Research Coordinator role. Our client, a leading research company, is looking to hire someone who can bring added value to the team. If you’re dedicated, energetic and detail-oriented, this could be the perfect role for you. Responsibilities include:

1) Coordinate clinical trials conducted by a supervising Principal Investigator in accordance with FDA, GCP and protocol guidelines.

2) Identify potential problems or inconsistencies and take action as appropriate.

3) Articulate protocol issues to CRO and Sponsor, Site Lead, Manager, Principal and Sub-Investigator, and other members of the study team

4) Collect initial subject health and demographic information by interviewing subjects and accessing other appropriate sources

5) Review subject comprehensive medical documentation to determine protocol eligibility under the supervision of the Principal Investigator

6) Ensure a flow of communication, including telephone conferences between subject, study staff, referral sources and recruitment team, Sponsor and CRO, monitor and auditors, if applicable

7) Perform clinical tasks including, but not limited to vital signs, height and weight, ECG, phlebotomy, specimen processing and packaging

8) Maintain timely internal source documentation as well as sponsor-required information

9) Maintain timely EDC data entry and query resolution

10) Maintain timely CTMS data entry of patient visits and study information

11) Complete verification of subjects before consenting

12) Report hospital census data, if applicable

13) Dispense and maintain accurate records of investigational and study product

14) Educate subject and family members regarding specific studies and clinical drug trials in general

15) Complete all monitor and sponsor queries in a timely manner

16) Perform quality control checks on all trials as per company SOP and interface with QA Director, as needed

17) Perform other duties as assigned

Critical Requirements

1) A university degree is required. Although all candidates are welcome and encouraged to apply, preference will be given to those with degrees in a relevant field

2) Appropriate full-time work experience is mandatory (no students or fresh graduates please)

3) Recent experience in the research industry is strongly preferred

4) Preference will be given to candidates with recent experience in clinical research coordinator

If you are qualified and this seems like just the right opportunity to take your career to the next level, please apply – we want to hear from you!

Compensation and Other Details

Base Salary: Highly competitive package, commensurate with experience


  • Published on 06 Feb 2023, 6:12 PM