Job Summary
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
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