Study Coordinator

Alpha Clinical Laboratory Inc; Fayetteville (NC); On-site; USD 60,000 - 90,000; Full time

Job summary

Alpha Clinical Laboratory Inc in Fayetteville, NC is seeking a Sr. Clinical Trial Site Coordinator to oversee daily trial operations, recruit and screen participants, obtain informed consent, and ensure protocol compliance.

You will collect and document data per GCP, liaise with investigators, sponsors, and monitors, manage study supplies, and safeguard participant safety while preserving data integrity.

Qualifications

• 5+ years of clinical research/site coordination experience.
• Experience with GCP and regulatory standards.

Responsibilities

• Recruit and screen participants, obtain informed consent, and ensure protocol compliance.
• Collect and document data accurately, maintaining records per GCP standards.
• Liaise with investigators, sponsors, and study monitors.
• Manage day-to-day operations of clinical trials at the site.
• Ensure timely execution of the trial, maintain study supplies, and safeguard participant safety.
• Maintain data integrity and safety of participants.

Job description

• Recruit and screen participants, obtain informed consent, and ensure protocol

Overview

Position summary

• Recruit and screen participants, obtain informed consent, and ensure protocol

compliance.

• Collect and document data accurately, maintaining records per GCP standards.
• Liaise with investigators, sponsors, and study monitors.

A Clinical Trial Site Coordinator will be responsible for managing the day-to-day operations of clinical trials at a specific site. Key responsibilities will include recruiting and screening participants, obtaining informed consent, and ensuring compliance with study protocols and regulatory requirements. They will manage patient visits, collect and document data accurately, and maintain proper records in line with Good Clinical Practice (GCP) standards. The coordinator will also liaise with investigators, sponsors, and study monitors, manage study supplies, and ensure the timely and efficient execution of the trial. Additionally, they will play a crucial role in maintaining the safety and well-being of participants while ensuring the integrity of the clinical data collected.

Job Nature

Contract, Onsite

Experience Requirements

5+

Job Location

Fayetteville, NC

Job Level

Sr. Position