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Clinical Research Coordinator


Phoenix, Arizona
  • Clinical Operations
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  • Research Salary

Job Details

Dear Clinical Research Coordinators,

I understand that you can find an opportunity anywhere you go. You are needed and necessary in Clinical Research however, companies have a big problem of not listening to YOUR needs and not valuing you as a person. As a Clinical Research Recruiter I have built a rapport with large and well known Clinical Research facilities. I actually partner with HR teams to get your resume in front of a hiring manager and talk with them about your wants and needs. I will fight for you and make sure that you are heard and that you are VALUED most importantly.

Position Summary of Clinical Research Coordinator:

You will be responsible for coordinating clinical research protocols from study start up to close out. This candidate will work closely with all research staff to collect, store and maintain data in accordance with FDA Regulations, International Council of Harmonization and Good Clinical Practices.

Job Responsibilities of a Clinical Research Coordinator:

-May be the sole coordinator or work in collaboration with a research nurse on studies, responsible for source documents, data collection, data entry, query resolution, triggering financial payments, study close out and liaison with the Sponsor/CRO.

-Participates in the identification of potential clinical trial participants, screens them for eligibility, and enrolls participants per protocol.

-Coordinates the schedule of events for clinical trial participants from screening to follow up according to protocol.

-Collects, verifies, organizes and records clinical information and data in electronic data capture systems (EDC). Abstracts data from necessary sources to complete the EDC and resolve queries. Performs the following data related activities. EDC tracking, reviewing validation, updating, SAE reconciliation, lab data reconciliation and safety coding.

Reference number: 58007