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Clinical Research Coordinator - Part Time
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
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