Senior Clinical Trials Coordinator - GCP & IRB Mastery

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

Benefits offered by this job

Medical insurance

Tuition assistance

Retirement plans

Job summary

Jefferson Health is seeking a clinical research professional to oversee day-to-day activities of trials from startup to closeout. You will coordinate protocol activities, manage data and biospecimens, and prepare regulatory/IRB documents to ensure GCP compliance.

The role includes training staff, developing workflows, and participating in cross-functional workgroups to optimize trial execution.

Qualifications

• High school diploma or GED required.
• 5 years clinical research experience with SoCRA 6 years total, or 2 years with a Bachelor's and 2 years experience, or 1 year with a Master’s and 1 year experience.

Responsibilities

• Oversee day-to-day activities of a clinical trial per GCP.
• Coordinate protocol activities: screening, enrollment, consent, and feasibility.
• Prepare regulatory and IRB documents; ensure protocol compliance.
• Train and supervise staff; contribute to workflow documentation.
• Manage data capture, biospecimens, and monitoring preparations.

Skills

GCP knowledge

Clinical trial coordination

IRB regulatory processes

Quality control & data management

Staff training & supervision

Education

Bachelor's degree in life sciences

Master's degree in health sciences

Tools

IRB submissions tools

Electronic data capture (EDC) systems

Job description

Jefferson Health is seeking a clinical research professional to oversee day-to-day activities of trials from startup to closeout. You will coordinate protocol activities, manage data and biospecimens, and prepare regulatory/IRB documents to ensure GCP compliance.

The role includes training staff, developing workflows, and participating in cross-functional workgroups to optimize trial execution.