Clinical Research Coordinator - Part Time
GULF COAST HEART AND VASCULAR LLC
Behavioral Health Market Context
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Job Description
nd 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
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
Qualifications
- •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
Benefits
- •Competitive salary based on experience
- •Opportunity for career growth
- •Direct exposure to sponsors and leadership
- •Flexible and collaborative work culture
Responsibilities
- •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
- •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
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