Clinical Research Coordinator — Onsite Contract to Perm

System One Clinical & Science; West Chester (Chester County); On-site; USD 36,000 - 41,000; Full time

Benefits offered by this job

Health benefits

401(k) plan

Job summary

System One Clinical & Science is seeking a Clinical Research Coordinator for an onsite contract position in West Chester, PA. The role involves coordinating protocols, screening participants, and assisting with informed consent under supervision.

The candidate will manage study visits, ensure data quality, and adhere to GCP/HIPAA guidelines. A health-related degree is preferred, with strong organizational and communication skills.

Qualifications

• Basic knowledge of clinical research is preferred.
• Experience with informed consent and patient enrollment is preferred.
• Proficiency with electronic data capture systems and trial management software.

Responsibilities

• Coordinate and execute clinical research protocols under supervision.
• Conduct screening visits and collect medical history.
• Assist with informed consent and enrollment of participants.
• Schedule study visits and follow-up activities with clinical teams.
• Maintain accurate study data and source documentation.

Skills

Clinical research basics

Electronic data capture

Microsoft Office

GCP/HIPAA knowledge

Communication with diverse populations

Education

High school diploma or equivalent

Associate’s degree or higher in health-related field (preferred)

Tools

Clinical trial management software

Job description

System One Clinical & Science is seeking a Clinical Research Coordinator for an onsite contract position in West Chester, PA. The role involves coordinating protocols, screening participants, and assisting with informed consent under supervision.

The candidate will manage study visits, ensure data quality, and adhere to GCP/HIPAA guidelines. A health-related degree is preferred, with strong organizational and communication skills.