Imaging Clinical Research Coordinator

Health Partners Plans; Philadelphia (Philadelphia County); On-site; USD 50,000 - 75,000; Full time

Job summary

Thomas Jefferson University is seeking a detail-oriented team member to oversee the day-to-day activities of clinical trials in compliance with GCP. The role involves data management, biospecimen processing, and clerical tasks to support investigators in organizing and compiling research data.

You will recruit and assist with subject consent, conduct study visits, and help ensure adherence to regulatory requirements.

Qualifications

• High School Diploma or GED required.
• 4 years of relevant experience.
• Experience with clinical trial processes.
• Knowledge of regulatory bodies affecting healthcare.
• Ability to manage multiple projects.

Responsibilities

• Interacts with co-workers and staff consistent with Jefferson values.
• Oversees day-to-day activities of a clinical trial and assists investigators with organizing and compiling data.
• Recruitment and consent assistance; conduct study visits as needed.
• Assist Principal Investigator with regulatory filings including IRB submissions.
• Provide clerical and technical support to ensure adherence to research protocols.

Skills

Clinical research

Data management

IRB submissions

Subject recruitment

Regulatory compliance

Documentation

Education

High School Diploma/GED or equivalent

Job description

Thomas Jefferson University is seeking a detail-oriented team member to oversee the day-to-day activities of clinical trials in compliance with GCP. The role involves data management, biospecimen processing, and clerical tasks to support investigators in organizing and compiling research data.

You will recruit and assist with subject consent, conduct study visits, and help ensure adherence to regulatory requirements.