Clinical Research Coordinator (CRC) – Infectious Disease

Vitalief•Franklin Township, NJ

20h•Onsite

About The Position

We are looking for an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full-time employee with comprehensive benefits. This role will support a non-interventional infectious disease clinical trial conducted at a community hospital site in Somerset, New Jersey, as part of a large pharmaceutical-sponsored study. The ideal candidate will have at least one (1) year of experience as a CRC, along with strong attention to detail, a genuine interest in clinical research, and the ability to work independently in a fast-paced environment. This role requires a proactive, self-starting individual who can effectively manage patient-facing responsibilities while ensuring strict adherence to protocol requirements, regulatory standards, and specimen handling procedures. The CRC will work closely with the Principal Investigator (PI) and site leadership to support the successful execution of the study.

Requirements

Bachelor’s degree required (healthcare, life sciences, or related field preferred).
Minimum of one (1) year of practical experience as a Clinical Research Coordinator.
Prior experience working as a CRC in an Academic Medical Center (AMC) or community hospital setting is strongly preferred.
Phlebotomy certification or willingness to learn phlebotomy.
Experience in infectious disease studies preferred.
Strong understanding of Good Clinical Practice (GCP) and clinical trial processes.
Demonstrated ability to work independently and manage multiple priorities.
Enthusiastic and motivated team player; Self-starter with the ability to take initiative.
Excellent organizational skills and high attention to detail.
Strong interpersonal and communication skills, with a patient-centered approach.
Ability to problem-solve and adapt in a dynamic clinical environment.
Proficiency with electronic data capture (EDC) systems and Microsoft Office.

Responsibilities

Coordinate and execute day-to-day clinical trial activities across both sites in accordance with the study protocol, GCP, and regulatory requirements.
Work closely with the Principal Investigator (PI) to support study oversight, patient eligibility review, safety reporting, and protocol adherence.
Identify, screen, and consent eligible patients for participation in the study.
Schedule and manage patient visits, ensuring protocol compliance and timely completion of study procedures.
Serve as the primary point of contact for study participants, including meeting patients during visits and conducting follow-up communications.
Accurately collect, document, and maintain study data in source documents and electronic systems.
Ensure proper specimen collection, processing, storage, and shipment in compliance with protocol and laboratory requirements.
Collaborate with investigators, site staff, and sponsor representatives to ensure smooth study conduct.
Monitor patient safety and report adverse events per protocol and regulatory guidelines.
Maintain regulatory binders and ensure audit readiness at all times.
Support monitoring visits, audits, and inspections as needed.