Clinical Trials Coordinator - Data, Recruitment & Visits

jeffersonhealth; Philadelphia (Philadelphia County); On-site; USD 60,000 - 90,000; Full time

Job summary

Jefferson Health in Philadelphia is seeking a Clinical Research Coordinator to support a compliant clinical trial under GCP. You will handle database management, biospecimen processing, and clerical tasks to assist investigators in organizing and compiling data.

You will recruit and assist with consenting subjects and conduct study visits. Responsibilities include coordinating with the Principal Investigator, maintaining regulatory filings, and ensuring accurate documentation while upholding

Qualifications

• High School Diploma or GED required.
• 4 years of relevant experience.
• Knowledge of database tools to organize, store and manage data.
• Understanding of healthcare regulations affecting clinical trials.
• Familiarity with patient rights and consent processes.

Responsibilities

• Oversee day-to-day activities of a clinical trial under GCP.
• Recruit and assist with consenting subjects and conduct study visits.
• Perform data management and biospecimen processing for trials.
• Maintain documentation and organize trial records.
• Coordinate regulatory filings including IRB submissions.

Skills

Database management

Biospecimen handling

Clerical tasks

Consent procedures

Study visits

Education

High School Diploma/GED

Tools

Database software

Job description

Jefferson Health in Philadelphia is seeking a Clinical Research Coordinator to support a compliant clinical trial under GCP. You will handle database management, biospecimen processing, and clerical tasks to assist investigators in organizing and compiling data.

You will recruit and assist with consenting subjects and conduct study visits. Responsibilities include coordinating with the Principal Investigator, maintaining regulatory filings, and ensuring accurate documentation while upholding