Senior Clinical Research Coordinator - Trials & Compliance

Jefferson Health; Alabama; On-site; USD 60,000 - 85,000; Full time

Job summary

Thomas Jefferson University seeks an experienced professional to oversee day-to-day clinical trial activities in accordance with Good Clinical Research Practice. You will coordinate protocol activities, manage data, prepare regulatory documents, and support staff training.

Responsibilities include IRB submissions, quality control of data, and creation of workflows to ensure protocol adherence and regulatory compliance in a dynamic research environment.

Qualifications

• Minimum: High School Diploma/GED.
• SoCRA certification or extensive clinical research experience preferred.
• Experience with protocol coordination, data management and regulatory documentation.

Responsibilities

• Oversees day-to-day activities of a clinical trial per GCP.
• Prepares and submits IRB/regulatory materials as required.
• Maintains trial documentation and subject logs; tracks visits and payments.
• Performs quality control on trial data and manages data storage.
• Designs/evaluates electronic data capture databases and supports staff training.

Skills

GCP knowledge

SoCRA Certification

Clinical research

Regulatory documentation

Education

High School Diploma / GED

Bachelor’s degree in life sciences or related field

Master’s degree (preferred)

Job description

Thomas Jefferson University seeks an experienced professional to oversee day-to-day clinical trial activities in accordance with Good Clinical Research Practice. You will coordinate protocol activities, manage data, prepare regulatory documents, and support staff training.

Responsibilities include IRB submissions, quality control of data, and creation of workflows to ensure protocol adherence and regulatory compliance in a dynamic research environment.