Clinical Trial Operations Lead: GCP, IRB & Data

Jefferson Health; Philadelphia (Philadelphia County); Hybrid; USD 65,000 - 90,000; Full time

Job summary

Thomas Jefferson University is seeking a clinical research professional to oversee day-to-day trial activities in accordance with GCP. Responsibilities include protocol coordination, screening, enrollment, consent, data management, and regulatory document preparation.

The role involves training staff, developing workflows, and contributing to SOP revisions, with work primarily at our Philadelphia campus.

Qualifications

• Must have either a High School Diploma/GED with 5 years of clinical research experience, or 6 years with SoCRA.
• Or 2 years of clinical research with a Bachelor’s degree.
• Or 1 year with a Master’s degree and 1 year clinical research experience.
• SoCRA Certification is an additional qualification.

Responsibilities

• Oversee day-to-day activities of a clinical trial per GCP.
• Coordinate protocol activities from startup to closeout.
• Prepare IRB submissions and regulatory documents as required.

Skills

GCP knowledge

IRB submission

Protocol coordination

Data management

Education

High School Diploma / GED

SoCRA Certification

Bachelor's degree

Master's degree

Job description

Thomas Jefferson University is seeking a clinical research professional to oversee day-to-day trial activities in accordance with GCP. Responsibilities include protocol coordination, screening, enrollment, consent, data management, and regulatory document preparation.

The role involves training staff, developing workflows, and contributing to SOP revisions, with work primarily at our Philadelphia campus.