Job Description

We are looking to add a full time Senior Clinical Research Coordinator to a growing team. This role is hybrid with a WFH option of 2 days per week. The ideal candidate is local to Philadelphia and will be interested in moving into a leadership or project manager type position down the road. This position is working directly with patients, managing the study process from start up through close out on a growing team working to help change the future of therapeutics.

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

Job Tags

Similar Jobs