Clinical Research Coordinator - Part Time

Job Description

Job 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

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.