Informed Consent Jobs

The Perelman School of Medicine seeks a Clinical Research Assistant B to support renal and hypertension clinical/translational studies at the Smilow Center through recruitment, specimen processing, regulatory support, and data management.

Support a clinical research team at MUSC by coordinating participant recruitment, conducting study visits and sample handling, and maintaining regulatory-compliant study documentation for addiction pharmacology trials.

Support NIH-funded urogynecology research at the University of Pennsylvania as a Clinical Research Coordinator A, coordinating patient recruitment, study visits, and data collection for investigator-initiated clinical trials.

Join AbbVie's governance team as a Data Governance - Compliance Specialist to ensure compliant consent and sample management across clinical and R&D programs while driving process improvements and cross-functional coordination.

Care Access is hiring a Clinical Research Assistant in Miami to support community-based clinical trials through specimen collection, participant engagement, and study operations.

Support a pragmatic clinical trial investigating a mindfulness-based pain management program by coordinating participant interactions, data collection, device setup, and study operations on a per-diem, hybrid basis at BMC.

Holy Cross Hospital is hiring an on-site Registered Nurse Clinical Research Associate to support oncology clinical trials by coordinating patient recruitment, data collection, regulatory compliance, and safety reporting.

Northwestern Medicine seeks a Senior Regulatory Coordinator to lead IRB submissions and regulatory oversight for complex stem cell transplant and cell therapy studies within the Autoimmune Diseases program.

Support and coordinate routine ophthalmology clinical research activities, including participant screening, consenting, data entry, and regulatory maintenance at Bascom Palmer Eye Institute.

Entry-level Clinical Research Coordinator to manage routine ophthalmology study activities, participant coordination, data capture, and regulatory documentation at Bascom Palmer Eye Institute.

Shriners Children’s Lexington is seeking an organized Clinical Research Coordinator 1 to manage regulatory documentation, recruit and consent pediatric participants, and ensure accurate data collection and compliance for clinical studies.

University of Kansas Medical Center is hiring a Clinical Research Assistant to perform participant assessments, manage study data, and support coordination for the Clinical Osteoarthritis Research Program.