Clinical Research Coordinator - Part Time

Bethany Medical Clinic

New York, NYPart-time

Behavioral Health Market Context

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Benefits

Part-Time | One Day per Week (On-Site)One consistent day per week (on-site)Supplemental incomePortfolio or semi-retired workBalance alongside another research or clinical roleCompetitive hourly compensation commensurate with experienceA highly organized, collaborative, and respectful research environment4 more items(s)

Qualifications

  • •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
  • •The opportunity to contribute meaningfully to clinical research without a full-time commitment
  • •Stable, predictable schedule with minimal administrative burden
  • •6 more items(s)

Responsibilities

  • •We are seeking a Certified Clinical Research Coordinator (CCRC) to join our growing clinical research site on a part-time basis (one day per week)
  • •This role is ideal for an experienced coordinator who values high-quality research, operational excellence, and schedule flexibility
  • •The CCRC will play a critical role in ensuring the ethical, regulatory, and operational integrity of clinical trials while supporting investigators, participants, and sponsors in a highly organized and patient-centered environment
  • •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
  • •7 more items(s)
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