Clinical Research Coordinator

Do you love Clinical Research and want your next career step to be someplace with a lot of upward mobility and growth potential? We are looking for a Clinical Research Coordinator to join our growing team! Competitive salary, and a comprehensive benefits package are offered including, medical, dental, vision and 401k.

Overview

The Clinical Research Coordinator (CRC) is responsible for overseeing the day-to-day operations of clinical research trials designed to test the safety and effectiveness of new drugs. The CRC plans and directs clinical research studies – working directly with patients to guide them successfully through the clinical trial process.

Duties

The CRC thoroughly understands all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator.

Communicates closely with the sponsor’s Clinical Research Associate (CRA) to facilitate the sponsor monitoring and data maintenance process.

The Clinical Research Coordinator completes all monitor and sponsor queries in a timely manner.

Track enrollment status of patients and ensure timely communication with patients regarding their study participation.

Assess eligibility of potential patients and oversee patient enrollment to ensure that informed consent is properly obtained and documented.

Coordinates and conducts patient visits (drawing blood, collecting vital signs, performing ECGs, and processing specimens).

Keeps all source documentation up-to-date

Education

Bachelor’s degree Preferred

Experience.

2 year of Clinical Research experience required

Ophthalmology experience preferred

Additional Skills for the Clinical Research Coordinator

Phlebotomy skills are a plus

Ability to work well both independently and as part of a team

Ability to handle multiple tasks simultaneously