Clinical Research Coord II
About the role
The position will coordinate and manage day-to-day operations of clinical research studies within the Lung Transplant Program; screen, recruit, consent, and enroll research participants in accordance with approved protocols and regulatory requirements; maintain compliance with Good Clinical Practice (GCP), institutional policies, sponsor guidelines, and applicable federal regulations.
Responsibilities
- Prepare and submit regulatory documents, including but not limited to Institutional Review Board (IRB) submissions, continuing reviews, amendments, and study closures.
- Cook up and coordinate study visits, specimen collection, and research-related procedures.
- Perform accurate and timely data collection, entry, verification, and database management.
- Maintain study files and regulatory binders and ensure completion of required study documentation.
- Aid investigators with protocol implementation and ongoing study management.
- Collaborate with multidisciplinary clinical and research teams across multiple locations.
- Participate in study monitoring visits, audits, and sponsor communications as needed.
Requirements
Ability to sit, stand, and walk for extended periods of time. Ability to travel between UPMC Presbyterian and UPMC Shadyside campuses. Ability to transport study materials and equipment as needed. Must have reliable transportation for travel between clinical and research sites.
Qualifications
- Bachelor's Degree
- 2+ years of relevant experience
Skills
Good Clinical Practice (GCP) compliance, regulatory document preparation, study visit coordination, data collection, and database management.
Benefits
N/A
Pay
To Be Determined Based On Qualifications
Schedule
Monday-Friday, 8:30 a.m. - 5:00 p.m.