The Site Manager will conduct ongoing outreach to clinical trial sites to ensure study progress, engagement, and adherence to expectations. They are responsible for managing site documentation, resolving action items, and supporting enrollment strategies across a portfolio of 30 to 40 sites.
Lead complex clinical research projects across the full trial lifecycle, including clinical operations, data, and regulatory submission needs. Manage study budgets, timelines, risks, and sponsor expectations to ensure successful project delivery.
The Senior Site Manager will oversee clinical trial site operations from feasibility through initiation, ensuring sites are prepared and compliant with study protocols. They will perform remote monitoring activities, including source data verification, while providing guidance and mentorship to team members.
The Statistical Programmer will own the statistical programming process, creating analysis datasets and programming tables, listings, and figures. They will interpret study protocols and ensure all outputs meet validation and quality standards in a regulated environment.
