Clinical Research Coordinator
Westlake, OHFull-time
Behavioral Health Market Context
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Qualifications
- •2+ years of experience as a Clinical Research Coordinator
- •Strong understanding of clinical trial processes, GCP, and regulatory guidelines
- •Excellent organizational skills and attention to detail
- •Ability to manage multiple studies and deadlines efficiently
- •Strong communication and interpersonal skills
- •Experience with EDC systems and clinical research software
- •Ability to work independently while being a team player
- •Experience across multiple therapeutic areas
- •Certification (CCRC, CCRP, or equivalent)
- •Prior experience working in a high-volume research environment
- •7 more items(s)
Responsibilities
- •We're seeking an experienced Clinical Research Coordinator who thrives in a fast-paced, detail-oriented environment and understands the importance of both precision and compassion
- •In this role, you won't just manage studies, you'll help bring life-changing treatments closer to reality while ensuring patients feel supported every step of the way
- •Coordinate and manage clinical trials from start-up through close-out
- •Serve as the main point of contact for study participants, ensuring a positive and professional experience
- •Screen, recruit, and consent eligible participants
- •Maintain accurate and timely documentation in compliance with protocols, GCP, and regulatory standards
- •Schedule and conduct study visits, collect data, and manage source documentation
- •Collaborate with investigators, sponsors, and CROs
- •Monitor patient safety and report adverse events appropriately
- •Ensure all study activities meet FDA and IRB requirements
- •7 more items(s)