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The Sr Site Activation Specialist will be responsible for facilitating clinical trial site activation processes, ensuring timely initiation and compliance with study protocols.

Support month-end, quarter-end, and year-end close activities; prepare journal entries, account reconciliations, and intercompany reconciliations; ensure compliance with US GAAP and Sarbanes-Oxley controls; analyze expenses and accruals; maintain Oracle/general ledger systems; assist with audits, process documentation, and continuous improvement initiatives; provide training and collaborate with international accounting teams.

Provide HR shared-services support including onboarding/offboarding, records management, benefits and compensation administration, HRIS data integrity, compliance with GDPR/SOX/local laws, root-cause analysis, SOP updates, and international HR support (visas, transfers). Collaborate with HR COEs and HRBPs, train and guide junior staff, and contribute to process improvements and People Operations projects.

The Safety & PV Specialist I is responsible for data entry and tracking of safety reports, maintaining compliance with SOPs, and conducting literature reviews related to safety in clinical trials.

The Principal-Global Feasibility Data Science role involves managing complex feasibility assessments independently and collaborating with various stakeholders to derive innovative solutions.

The Sr. Statistical Programmer develops programming code using SAS to generate statistical outputs, ensures quality standards, manages multiple projects, and leads programming teams. Responsibilities include documentation, communication with teams, and mentoring programming personnel while participating in sponsor meetings.

Responsible for processing and tracking individual case safety reports (ICSRs), maintaining safety tracking, and ensuring compliance with safety regulations in pharmacovigilance.

The Project Associate will drive project planning and execution, coordinate resources, monitor project performance, and manage communications in clinical trials.

The Safety & PV Specialist I role involves processing ICSR data, maintaining safety tracking systems, conducting literature reviews, and ensuring compliance with safety reporting regulations.

The CRA will monitor clinical research studies for compliance, develop tools for quality monitoring, manage project components, and collaborate with teams to ensure effective clinical trial operations.