Sarah Cannon Research Institute jobs

Manages regulatory operations and ensures FDA compliance for site Clinical Operations.

• Remote · Tennessee, United States or North America
• 1+ yrs

Drives product and business analysis to enable digital transformation in healthcare.

• Remote · Texas or United States
• 3+ yrs

Directs design, plan, delivery and evaluation of clinical trial training activities for SCRI colleagues.

• Remote · Nashville or United States

Manages multiple clinical projects from initiation to closeout across lifecycle phases.

• Remote · Tennessee or United States
• Senior

Manages regulatory compliance activities for conflicts of interest in clinical studies.

• Remote · Nashville or United States

Provides pharmacovigilance and safety monitoring for patients in clinical trials.

• Nashville, United States · Hybrid

Ensures the Trial Master File is set up and maintained in audit-ready condition and supports documentation collection throughout the study.

• Remote · Tennessee, United States or North America
• 1+ yrs

Coordinate blood cancer and bone marrow transplant clinical trials and data across study sites.

• Denver, United States · On-site
• 1+ yrs

Plan, execute and monitor complex clinical research protocols across phases I–IV.

• Nashville, United States · Hybrid
• 1+ yrs

Follow study subjects and ensure protocol compliance and close monitoring.

• Nashville, United States · On-site
• 1+ yrs