Senior Clinical Research Coordinator: GCP & IRB Lead

Jefferson Health; Philadelphia (Philadelphia County); On-site; USD 65,000 - 98,000; Full time

Benefits offered by this job

Medical insurance (including Rx)

Dental and Vision insurance

Retirement plans

Job summary

Jefferson Health is seeking a dedicated professional to oversee daily clinical trial activities in accordance with Good Clinical Practice (GCP). The role spans startup to closeout, including protocol coordination, data management, regulatory document preparation, and staff training.

You will ensure all procedures align with protocol and regulations while supporting workflow improvements. The candidate will contribute to IRB submissions, quality control, and data integrity, with opportunities to

Qualifications

• High School Diploma or GED required.
• SoCRA Certification required or equivalent credential.
• 2–6 years of clinical research experience depending on degree.

Responsibilities

• Oversee day-to-day activities of a clinical trial per GCP.
• Coordinate protocol activities from startup to closeout.
• Prepare regulatory submissions and IRB materials as required.
• Maintain accurate subject logs and data management.
• Train and supervise staff; assist in workflow development.

Education

SoCRA Certification

Job description

Jefferson Health is seeking a dedicated professional to oversee daily clinical trial activities in accordance with Good Clinical Practice (GCP). The role spans startup to closeout, including protocol coordination, data management, regulatory document preparation, and staff training.

You will ensure all procedures align with protocol and regulations while supporting workflow improvements. The candidate will contribute to IRB submissions, quality control, and data integrity, with opportunities to