Clinical Research Coordinator II — Trials & Compliance

Cenexelresearch; Marlton (NJ); On-site; USD 36,000 - 47,000; Full time

Job summary

CenExel Clinical Research in Marlton, NJ is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials with strict adherence to ICH, GCP, protocol, and company guidelines. This full-time role manages data collection and regulatory duties, with compensation of $26.24-$33.51 per hour.

The ideal candidate will have 2–3 years in the medical field, strong communication, and ability to work independently as part of a multidisciplinary team.

Qualifications

• Must have mastery of Clinical Research Coordinator I responsibilities.
• Bachelor's degree preferred; CCRC certification preferred.
• 2-3 years of experience in the medical field recommended.

Responsibilities

• Coordinate all aspects of patient involvement for complex studies from initiation to completion.
• Organize research information for clinical trials and monitor data collection.
• Observe subjects and assist with data analysis and reporting; manage data collection schedules.
• Review and report adverse events, protocol deviations, and other issues.
• Ensure regulatory duties and sponsor/vendor communications are maintained.

Skills

Leadership

Mentorship

Communication

Regulatory knowledge

Education

High school diploma or equivalent; Bachelor's degree preferred

CCRC certification preferred

2-3 years of experience in medical field

Job description

CenExel Clinical Research in Marlton, NJ is seeking a Clinical Research Coordinator I to coordinate all aspects of clinical trials with strict adherence to ICH, GCP, protocol, and company guidelines. This full-time role manages data collection and regulatory duties, with compensation of $26.24-$33.51 per hour.

The ideal candidate will have 2–3 years in the medical field, strong communication, and ability to work independently as part of a multidisciplinary team.