Clinical Research Coordinator iCTS Holdings LLC Fort Lee, NJ 07024 Hybrid work $30
- $35 an hour
- Full-time, Contract $30
- $35 an hour
•
Full-time, Contract Job Description:
The Clinical Research Coordinator (CRC) will support and coordinate clinical trials conducted within the Clinical Trials Office. The CRC is responsible for managing day-to-day trial activities, ensuring compliance with study protocols, regulatory requirements, and institutional policies. This role involves working closely with investigators, sponsors, and study participants to facilitate high-quality and ethical clinical research.
Key Responsibilities:
Coordinate and manage clinical trial activities from initiation to close-out. Recruit, screen, and enroll study participants according to protocol eligibility criteria. Obtain informed consent and ensure adherence to Good Clinical Practice (GCP). Collect, record, and maintain accurate study data and documentation. Schedule and conduct study visits and follow-up assessments. Communicate with investigators, sponsors, and regulatory bodies. Prepare for and participate in monitoring visits, audits, and inspections. Ensure timely reporting of adverse events and deviations.
Qualifications:
Bachelor's degree in a health-related field (required); clinical research certification preferred. 1-3 years of experience in clinical research or healthcare setting. Knowledge of
ICH-GCP, NAFDAC
regulations, and IRB requirements. Strong organizational and communication skills. Ability to work independently and as part of a team.
Pay:
$30.00
00 per hour
Benefits:
Flexible schedule
Language:
Spanish (Required)
Work Location:
Hybrid remote in Fort Lee, NJ 07024