Bethany Medical Clinic of New York, PLLC ยท 3 days ago
Clinical Research Coordinator - Part Time
Bethany Medical Clinic of New York is seeking a Certified Clinical Research Coordinator (CCRC) to join their growing clinical research site on a part-time basis. The CCRC will ensure the ethical, regulatory, and operational integrity of clinical trials while supporting investigators, participants, and sponsors in a highly organized environment.
ConsultingHealth Care
Responsibilities
Coordinate and manage assigned clinical trials in compliance with GCP, ICH, FDA regulations, and IRB requirements
Serve as the primary point of contact for study participants, investigators, sponsors, and CROs on assigned study days
Conduct study visits, including participant screening, informed consent, visit coordination, and protocol-specified procedures
Ensure accurate, timely, and complete documentation in source documents, EDC systems, and regulatory binders
Support monitoring visits, audits, and inspections, ensuring readiness and responsiveness
Maintain study supplies, investigational product accountability, and specimen handling per protocol
Collaborate closely with the Principal Investigator and research leadership to support study success
Qualification
Required
Certified Clinical Research Coordinator (CCRC) required
Minimum 2+ years of hands-on clinical research coordination experience
Strong working knowledge of GCP, ICH, FDA regulations, and IRB processes
Experience working directly with sponsors, CROs, and monitors
Excellent organizational skills with high attention to detail
Professional, patient-centered communication style
Ability to work independently and efficiently in a focused, one-day-per-week role
Preferred
Experience in industry-sponsored clinical trials
Familiarity with EDC platforms (e.g., Medidata, REDCap, Veeva, or similar)
Experience across multiple therapeutic areas (not required)
Benefits
A highly organized, collaborative, and respectful research environment.
The opportunity to contribute meaningfully to clinical research without a full-time commitment.
Stable, predictable schedule with minimal administrative burden.