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The Clinical Site Manager at Parexel oversees clinical trial sites, ensuring compliance, managing interactions with site staff, and addressing issues throughout study phases.

Lead CMC regulatory projects and develop strategies for drug approval, ensuring compliance and liaising with clients and regulatory authorities.

The Senior Business Development Director will drive new business acquisition, maintain client relationships, and collaborate on strategic sales plans. Responsibilities include understanding client needs, ensuring effective proposal strategies, and influencing decision-makers to achieve sales goals in a competitive environment.

As a Statistical Programmer I at Parexel, you will support clinical trial development by utilizing statistical programming to analyze data and contribute to project success.

The Manager, Project Planner coordinates project schedules, manages resources, and ensures timely deliverables by collaborating with cross-functional teams in clinical and commercial settings.

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 Regulatory Affairs Associate monitors and analyzes regulatory changes, translating them into actionable insights, supports strategic decision-making, and engages in industry networking.

The Clinical Research Associate II is responsible for maintaining study integrity and compliance, managing site relationships, resolving site issues, and ensuring timely completion of project goals in line with clinical trial protocols.

The role involves developing regulatory strategies, managing PMDA consultations, and leading regulatory submissions related to clinical development for pharmaceutical companies in Japan.

The Senior CRA ensures quality site management and monitoring of clinical trials, addressing protocol-related issues while maintaining compliance and investigator relations.