Clinical Research Coordinator - Part Time
Bmcofny
·Jan 7, 2026
- Salary
- $48 – $52/hr
- Location
- New York, New York
- Workplace
- Onsite
- Type
- Part-time
- Department
- Healthcare
- Experience
- 2+ years
- Source
- BetterTeam
Description
Job Title: Certified Clinical Research Coordinator (CCRC)
Part-Time | One Day per Week (On-Site)
Location:
Manhattan Clinical Research
222 East 31st street, second floor, New. York, NY 10016
222 East 31st street, second floor, New. York, NY 10016
Position Overview:
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.
Key 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.
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.
Preferred Experience:
- Experience in industry-sponsored clinical trials.
- Familiarity with EDC platforms (e.g., Medidata, REDCap, Veeva, or similar).
- Experience across multiple therapeutic areas (not required).
Schedule & Commitment:
- One consistent day per week (on-site).
- Ideal for professionals seeking:
- Supplemental income.
- Portfolio or semi-retired work.
- Balance alongside another research or clinical role.
What We Offer:
- Competitive hourly compensation commensurate with experience.
- 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.
How to Apply:
Please submit your CV and a brief cover note highlighting your clinical research experience and availability.
Skills
GCPClinical TrialsFDACompliance