"Clinical Research Coordinator C"

Job Description Summary

The Functional and Metabolic Imaging Group (FMIG), part of the Department of Radiology at the Perelman School of Medicine, is seeking a full-time Clinical Research Coordinator-C to support advanced clinical research focused on pulmonary imaging using investigational contrast agents, including Hyperpolarized Xenon-129. These studies are conducted under FDA IND/IDE oversight in partnership with industry sponsors.

The CRC-C will be primarily responsible for coordination and execution of human subject research visits, including obtaining informed consent in accordance with GCP standards and completing protocol-required source documentation and case report forms (CRFs). Outside of subject visits, the CRC-C will support recruitment, scheduling, and coordination logistics; request and upload medical records into EPIC; and assist with maintaining accurate documentation across institutional and sponsor systems.

The ideal candidate will bring prior experience supporting clinical trials under FDA IND or IDE oversight, particularly those involving investigational imaging agents or contrast materials. In addition to operational duties, the CRC-C will provide input from a study coordination perspective on protocol feasibility, grant planning, and development of regulatory materials, working collaboratively with investigators and other research staff to ensure documentation aligns with institutional and federal expectations. This role is well suited for a detail-oriented and experienced coordinator interested in contributing to a growing research program in advanced MRI-based lung imaging.

Position is contingent upon continued funding.

Job Responsibilities

• The Functional and Metabolic Imaging Group (FMIG), part of the Department of Radiology at the Perelman School of Medicine, is seeking a full-time Clinical Research Coordinator-C to support advanced clinical research focused on pulmonary imaging using investigational contrast agents, including Hyperpolarized Xenon-129. These studies are conducted under FDA IND/IDE oversight in partnership with industry sponsors. The CRC-C will be primarily responsible for coordination and execution of human subject research visits, including obtaining informed consent in accordance with GCP standards and completing protocol-required source documentation and case report forms (CRFs). Outside of subject visits, the CRC-C will support recruitment, scheduling, and coordination logistics; request and upload medical records into EPIC; and assist with maintaining accurate documentation across institutional and sponsor systems. The ideal candidate will bring prior experience supporting clinical trials under FDA IND or IDE oversight, particularly those involving investigational imaging agents or contrast materials. In addition to operational duties, the CRC-C will provide input from a study coordination perspective on protocol feasibility, grant planning, and development of regulatory materials, working collaboratively with investigators and other research staff to ensure documentation aligns with institutional and federal expectations. This role is well suited for a detail-oriented and experienced coordinator interested in contributing to a growing research program in advanced MRI-based lung imaging.
• Position is contingent upon continued funding.

Qualifications

• Bachelor of Science and 4 to 6 years of experience or equivalent combination of education and experience is required.

Job Location - City, State

Philadelphia, Pennsylvania

Department / School

Perelman School of Medicine

Pay Range

$62,000.00 - $67,794.79 Annual Rate