Jobs at Parexel

The Clinical Research Associate is responsible for managing and monitoring clinical trial sites to ensure patient safety and quality compliance. Responsibilities include site management, resolving protocol issues, and maintaining investigator relationships.

The Clinical Trial Leader is responsible for planning, conducting, and closing clinical trials, ensuring compliance with regulations, and leading cross-functional teams to meet trial goals. They manage trial budgets, oversee vendor interactions, and contribute to strategy development while fostering a collaborative team environment.

Lead site activation for clinical trials, ensuring studies are on time and meet quality standards. Oversee milestones, manage risks, and guide teams across multiple studies.

The Senior Tax Analyst will oversee corporate income tax compliance, prepare tax returns, assist with payments, and monitor indirect tax changes.

The Sr. Contracts Specialist amends, negotiates, and finalizes project budgets and contractual documents, ensuring quality deliverables and client interactions for Parexel's projects.

The Senior Study Contract Manager is responsible for negotiating and managing contracts and budgets for clinical trials, ensuring compliance with guidelines and facilitating communication with stakeholders.

The Regulatory Affairs Consultant guides clinical studies through regulatory requirements, advising teams on compliance and strategies for efficient trial execution. They engage with health authorities, manage communication, and ensure quality documentation.

The Senior Clinical Research Associate manages clinical trial sites, ensures adherence to regulations, oversees study conduct, and resolves issues while safeguarding patient safety.

The Senior Regulatory Consultant will oversee regulatory strategies, manage complex timelines, enhance team performance, and guide regulatory projects to support the development of transformative therapies.

As a Senior/Principal Regulatory Compliance Consultant, you will lead client engagements in QC Microbiology and sterile drug manufacturing, ensuring compliance and quality improvements while traveling extensively to support clients.

The Senior Clinical Research Associate oversees site management and monitoring for clinical trials, ensuring compliance with GCP, patient safety, and quality execution of studies. Responsibilities include managing operational aspects, training site personnel, addressing protocol issues, and conducting monitoring activities.

The Senior Clinical Research Associate is responsible for site management and monitoring of clinical trials, ensuring compliance with regulations and quality standards, and enhancing investigator site relationships.

The Senior Clinical Trial Manager oversees operational aspects of clinical trials from start-up to database lock, ensuring compliance with GCP and SOPs, managing vendors, and coordinating trial activities and communications with stakeholders.