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The Sr. Data Analyst performs data management tasks, supports CRM implementations, and resolves data issues, ensuring data readiness for field launch.

The R/SAS Statistical Programmer develops codes in R and SAS for statistical analysis, manages programming projects, conducts validation, and mentors junior programmers while adhering to CDISC standards.

The internship entails supporting APAC initiatives, creating content, preparing presentations for meetings, collaborating with colleagues, attending events, and assisting with administrative tasks.

The Sr Data Scientist will design methods for analyzing big data, develop software programs, mentor junior team members, and deliver insights for business goals.

Coordinate clinical trial processes, ensuring compliance and safety. Manage patient communication and documentation, while adapting to regulatory requirements and team collaboration.

The IMS Reporting Specialist II provides analytical support, oversees reporting and compliance, manages study invoicing, and collaborates with teams to ensure accurate data and timely reporting.

Conduct monitoring of clinical research studies, ensure compliance with GCP guidelines, manage project components, and collaborate with teams.

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

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.