Clinical Research Coordinator Part Time
GULF COAST HEART AND VASCULAR LLC, Panama City, FL, United States
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 systemsPhlebotomy 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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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 systemsPhlebotomy 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
#J-18808-Ljbffr