A company is looking for a Senior Site Management Associate to oversee site management activities for clinical trials.
Key Responsibilities
Oversee day-to-day site management activities to ensure compliance with study protocols and regulatory requirements
Collaborate with site staff and cross-functional teams to monitor progress and ensure timely data collection
Assist with site initiation, monitoring visits, and close-out activities while providing guidance to junior staff
Required Qualifications
Bachelor's degree in life sciences, clinical research, or a related field
Extensive experience in site management or clinical operations within the clinical research industry
Strong understanding of clinical trial processes and Good Clinical Practice (GCP)
Ability to manage multiple sites and timelines effectively
Experience in preparing site management documentation and reports
Management Associate • Lincoln, Nebraska, United States