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