Clinical Research Coordinator

Clinical Research Coordinator (CRC)

Location: Marlton, NJ

Schedule: Full-time, On-site | Monday–Friday, 8:30 AM – 5:00 PM

Overview:

Seeking a CRC with 1+ year of industry experience to coordinate clinical trials in compliance with ICH, GCP, and protocol guidelines. Must be comfortable working with psychiatric patients and performing EKGs, patient visits, and SIVs (no phlebotomy).

Key Responsibilities:

• Coordinate patient involvement from study start-up to completion.
• Assist with source documentation, training, and site initiation visits.
• Screen and enroll participants, ensuring protocol compliance.
• Conduct safety assessments (vital signs, EKGs, etc.) and manage drug accountability.
• Document subject data and report AEs, SAEs, and protocol deviations.
• Support monitoring visits and maintain professional communication with sponsors.

Qualifications:

• 1+ year CRC experience in clinical research.
• Strong understanding of ICH/GCP and federal regulations.
• Effective communicator with strong problem-solving skills.
• Comfortable working independently and in a team setting.

Work Environment:

• Large site (~130 staff) with inpatient and outpatient studies.
• Therapeutic areas include psychiatry, diabetes, vaccines, Alzheimer’s, and more.

Employee Value Proposition:

Opportunity for long-term career growth in clinical research.