Clinical Research Coordinator II: Recruitment & Biospecimens

University of Louisville; États-Unis; Sur place; USD 24 000 - 36 000; Temps partiel

Résumé du poste

University of Louisville is seeking a Clinical Research Coordinator II to support the Department of Surgery in multiple clinical studies. You will lead participant recruitment, screening, consent, enrollment, and biospecimen collection, ensuring protocol adherence and participant safety.

The role requires collaboration with investigators, clinical staff, and laboratory personnel to ensure accurate data collection, processing, and document management according to SOPs and regulatory standards.

Qualifications

• High School Diploma or GED plus 2+ years of relevant experience or equivalent education/experience.
• Experience coordinating participant recruitment, consent, and retention is preferred.
• Familiarity with biospecimen handling and data documentation is a plus.

Responsabilités

• Coordinate recruitment, screening, enrollment, and retention for multiple clinical studies.
• Identify eligible participants in inpatient and outpatient settings.
• Obtain informed consent and maintain ongoing communication with participants.
• Collect, label, store, and transport biological specimens per protocol and policy.
• Maintain chain-of-custody and timely delivery of samples to labs.
• Ensure study activities comply with IRB, GCP, and regulatory requirements.
• Maintain accurate study documentation and logs.
• Assist with regulatory documents and IRB submissions as needed.
• Communicate study requirements and schedules with investigators and teams.

Connaissances

Participant recruitment

Informed consent

Data collection & documentation

Formation

High School Diploma/GED

Description du poste

University of Louisville is seeking a Clinical Research Coordinator II to support the Department of Surgery in multiple clinical studies. You will lead participant recruitment, screening, consent, enrollment, and biospecimen collection, ensuring protocol adherence and participant safety.

The role requires collaboration with investigators, clinical staff, and laboratory personnel to ensure accurate data collection, processing, and document management according to SOPs and regulatory standards.