Onsite Part-Time Clinical Research Coordinator

Advarra; New Jersey; On-site; USD 34,000 - 55,000; Part time

Job summary

Advarra in New Brunswick, NJ, seeks a part-time Clinical Research Coordinator to support patient appointment coordination, data entry, and enrollment activities on-site. You will work with clinical technicians and research staff to ensure protocol adherence and regulatory compliance.

The ideal candidate has a degree with clinical research experience, includes phlebotomy with specimen handling, and familiarity with EDC systems, GCP guidelines, and trial coordination across multiple studies.

Qualifications

• Bachelor’s degree with 3+ years of relevant experience OR associate’s degree with 4+ years of experience.
• Phlebotomy experience with handling clinical specimens.
• Experience with patient scheduling, visit coordination, EDC data entry, and regulatory documentation.

Responsibilities

• Perform accurate and timely data entry and maintain study-related records.
• Coordinate patient appointments and facilitate clinical trial visits
• Support study enrollment and follow-up/closeout activities
• Collaborate with coordinators, clinical technicians, clinical research lead, and other research staff.
• Maintain compliance with regulatory requirements

Skills

Phlebotomy

Patient scheduling

Data entry

Regulatory documentation

Clinical trial coordination

Education

Bachelor’s or Associate degree with related experience

Tools

EDC software

Trial management systems

Job description

Advarra in New Brunswick, NJ, seeks a part-time Clinical Research Coordinator to support patient appointment coordination, data entry, and enrollment activities on-site. You will work with clinical technicians and research staff to ensure protocol adherence and regulatory compliance.

The ideal candidate has a degree with clinical research experience, includes phlebotomy with specimen handling, and familiarity with EDC systems, GCP guidelines, and trial coordination across multiple studies.