Clinical Research Coordinator - Part Time

Job Description

Job Description

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:

• Bachelors 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