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The Site Monitor II role involves ensuring data integrity, compliance, and quality at clinical sites through monitoring, training, and problem-solving. Responsibilities include site visits, documentation management, and collaboration with site staff to meet project goals and compliance standards.

The Principal Statistical Programmer leads statistical programming efforts for clinical trials, managing timelines, resources, and quality control of programming outputs while ensuring compliance with regulatory standards.

The Senior Biostatistician coordinates project teams, interacts with clients on statistical issues, performs quality control of data, and applies advanced statistical methods to clinical trials. They also support business development through study design input, budget proposals, and client meetings.

The Study Recruiter manages volunteer recruitment for clinical studies, coordinating calls, scheduling, and ensuring compliance with protocols.

The Senior Clinical Research Associate manages site monitoring and relationships for clinical trials, ensuring compliance and patient safety according to GCP and regulations.

The Senior CRA ensures compliance with regulatory standards, oversees site performance, manages data accuracy, and coordinates with local investigators for clinical trials.

The Investigator Contracts Lead will oversee the negotiation and execution of global clinical study agreements, manage budgets, and collaborate with legal and financial stakeholders to improve contracting processes.

The APEX CRA supports clinical research by assisting CRAs with project tasks and site-related responsibilities while gaining practical experience in clinical trials.

The role involves leading SKDL operations, managing processes, supporting data integrity, and enhancing communication with stakeholders in clinical research.

The Vice President, AI Enablement oversees AI strategy at Parexel, leading implementation across clinical and corporate functions while ensuring compliance and innovation.