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The Study Operations Manager I (SOM I) is responsible for study-specific country-level activities from study startup through conduct and study close on studies of limited complexity. The role requires expertise in leading clinical trials, study start-up, comprehensive knowledge of study management, and experience in managing country-level operational activities and vendors.

Manage a team of data engineers and support staff to design, build, and support data pipelines using Microsoft Azure data services. Create prototypes, run tests, benchmark application code, and collaborate with various teams for issue resolution and troubleshooting. Additionally, mentor technical staff and oversee technical delivery within the ecosystem.

The Senior Quality Assurance Auditor at Parexel is responsible for leading, planning, scheduling, performing, and reporting a range of GxP audits across all phases of Clinical Research. They must have a minimum of 2 years' experience in quality assurance, auditing, and at least 5 years' experience in relevant areas of life science. The role requires international travel for audits and a deep understanding of Good Practices (GxPs) and regulations related to clinical trials.

Principal Statistical Programmer responsible for project management, statistical programming for assigned projects, training, and general tasks. Provide leadership, ensure quality control, and compliance with regulations. Represent the company at sponsor meetings.

Design, build, modify, and support data pipelines using Microsoft Azure data PaaS services. Collaborate with Team Leads and QA Team. Implement test-driven development and continuous integration processes.

The Biostatistician II at Parexel independently leads the development and execution of statistical aspects for studies of low to moderate complexity. Responsibilities include protocol reviews, data interpretation, trial design, statistical consultation, and ensuring quality in planning and execution. The role requires a Master's degree in Statistics or equivalent with at least 3 years of industry-related experience.

The Statistical Programmer II provides technical expertise for the conduct of clinical trials, works with minimal supervision to support programming activities related to the analysis and reporting of clinical study data, and may fill the Statistical Programming Lead role on small projects. Responsibilities include project management, statistical programming for assigned projects, training, and general tasks related to regulatory compliance and quality improvement.