LiveHire users cookies on this website. Cookies are small pieces of data stored by your browser on your computer or device to help run this site, improve security, and improve your experience.

Click Accept to continue, or for more information please see our Cookies Policy.

‹ Back to all jobs

Clinical Research Coordinator

  • LocationPlano, TX 75024 - United States
  • Work TypeFull time
  • Positions1 Position
  • Published At:4 days ago
  • Job no: 39972
  • Category: Clinical

Job Description


Our client, a leading research company, is currently seeking an accomplished Clinical Research Coordinator to join the team. Here is an overview of the role:


1) Coordinate clinical trials conducted by a supervising principal investigator in accordance with FDA, GCP and protocol guidelines

2) Identify potential problems and 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

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 subjects 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 per company SOP and interface with the QA Director, as needed

17) Send all users email upon enrollment activation and closure

18) Participate in recruitment planning meetings prior to study start

19) Provide weekly updates to active studies report

20) Communicate all advertising needs to the Recruitment Team

21) Maintain weekly communication with the Recruitment Team in order to maximize recruitment in all enrolling trials

22) Communicate the need for study and company flyers

23) Read, understand and adhere to organizational SOPs

24) Assist in establishing and enforcing departmental standards contributes to team effort by working with internal staff to resolve issues

25) Explore new opportunities to add value to the organization and departmental processes

26) Help others at the site to achieve site goals

27) Perform other duties as assigned


Critical Requirements


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

2) Recent experience in the research industry is strongly preferred

3) Preference will be given to candidates with recent experience in clinical research coordination


This role is a great opportunity for the right person looking to advance their career with a wonderful company. If you are qualified and think that you are a strong fit for this role, please apply ASAP!


Compensation and Other Details


Base Salary: Highly competitive package, commensurate with experience

  • Published on 13 Jan 2022, 9:22 AM