Position Overview

We are seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) to join our team. The CRC will be responsible for the day-to-day coordination and execution of clinical trials, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP).

This is an excellent opportunity for someone who thrives in a startup environment and is eager to grow with an organization.

Key Responsibilities

Coordinate and manage clinical trials from start-up through close-out

Screen, recruit, and consent study participants

Schedule and conduct study visits per protocol

Collect, process, and ship laboratory specimens

Accurately document study data in source documents and electronic data capture (EDC) systems

Ensure compliance with FDA regulations, ICH-GCP guidelines, and study protocols

Maintain regulatory binders and essential documents

Communicate with sponsors, CROs, and study monitors

Prepare for and participate in monitoring visits, audits, and inspections

Track study timelines, enrollment, and patient follow-up

Report adverse events and protocol deviations appropriately

Qualifications

Required:

Bachelor’s degree in health sciences, biology, or related field (or equivalent experience)

1+ years of clinical research experience (or strong clinical background willing to train)

Knowledge of GCP and FDA regulations

Strong organizational and multitasking skills

Excellent communication and interpersonal skills

Ability to work independently in a fast-paced environment

Preferred:

Experience in cardiology

Experience with EDC systems

Phlebotomy and/or clinical skills

ACRP or SOCRA certification (or willingness to obtain)

What We Offer

Competitive salary based on experience

Opportunity for career growth

Direct exposure to sponsors and leadership

Flexible and collaborative work culture