Clinical Research Coordinator

On-site role based in Oklahoma City, OK.

The Study Coordinator coordinates clinical research program by identifying and assessing patients, distributing information, acting as a clinical resource, conducting follow-up care for patients, attending meetings pertaining to the clinical trial.

SUMMARY

Assist in the daily operation of clinical trials by coordinating clinical research studies according to site SOPs and GCPs.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following.

· Conducts clinical research studies according to study sponsor requirements as well as FDA guidelines and ICH/GCPs guidelines.

· Provide documentation of all study procedures conducted in a clinical trial.

· Recruit and maintain patients in assigned studies.

· Perform necessary protocol-related procedures.

· Screen potential patients both via phone and in office.

· Maintain adequate study medication documentation.

· Keep doctors updated on the patient’s status and any changes in the patient’s medical condition that the patient has not reported to the doctor.

· Primarily office and non-manual work directly related to the business operations of the employer

· Exercises discretion and independent judgment with respect to matters of significance

QUALIFICATIONS

BS, BA, or LPN preferred. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.