Research Patient Coordinator

Monroe+Biomedical+Research•North Charleston, SC

34d•Onsite

About The Position

At Monroe Biomedical Research, our Research Patient Coordinators or CRC play a critical role in the successful execution of clinical trials and the advancement of innovative medical treatments. This position combines patient interaction, clinical procedures, data management, and study coordination in a fast-paced research environment. We are seeking a motivated, detail-oriented professional who enjoys working directly with patients, collaborating with clinical teams, and contributing to high-quality research operations.

Requirements

Associate degree or equivalent experience required
Strong organizational skills and ability to manage multiple priorities
Professional communication skills and strong attention to detail
Comfortable working independently while collaborating within a team environment

Nice To Haves

Bachelor’s degree preferred
Prior healthcare experience strongly preferred
Experience in clinical research, patient care, medical assisting, or nursing preferred

Responsibilities

Coordinate and schedule participant visits for active clinical studies
Maintain study workflows and source documentation in accordance with sponsor protocols and regulatory requirements
Support overall study execution to ensure timelines and quality standards are met
Build positive relationships with study participants and provide ongoing support throughout study participation
Perform study-related procedures including: Vital signs, ECGs, Blood collection/phlebotomy, Pulmonary function testing
Assist in ensuring participant safety, comfort, and protocol compliance
Review medical records and maintain accurate clinical documentation
Enter and manage study data within sponsor systems
Prepare, process, and ship laboratory specimens according to protocol requirements
Assist with regulatory and sponsor documentation as needed