Join Our Team as a Clinical Research Coordinator!

UpTrials, in partnership with Crox, is a new job seeker platform to help clinical research job seekers get hired into the industry quickly.
We are seeking a full-time, experienced Clinical Research Coordinator. The Research Coordinator will facilitate all facets of Gastrointestinal clinical research studies.

Responsibilities:
Administratively and clinically manage industry-sponsored clinical trials
Adhere to Research SOP’s, Good Clinical Practices, and the study protocols
Participate actively in communication of status and results to senior management
Assist in training site personnel in regulatory, lab procedures, and general study-related training
Assist in patient recruitment by performing detailed chart reviews and patient interviews
Discuss study protocols with patients and verify the informed consent documentation
Review medical history of patients against Inclusion/Exclusion Criteria of studies
Perform blood draws, process and ship blood/urine specimens per study protocol and IATA regulations
Schedule all patient research visits and procedures consistent with protocol requirements
Dispense study medication, collect vital signs and perform ECGs
Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol
Ensure the filing and maintenance of all regulatory documents
Schedule and prepare for monitor visits
Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy
Maintain contact with clients and resolve any issues or questions for which the client made inquiries
Assist with Practice focus on improving patient satisfaction and the patient experience
Assist in preparing a brief monthly report on key indicators and issues

Medical Assistant or LPN required, Associates degree in a clinical or scientific-related discipline preferred