Posted Jul 12, 2026

Clinical Development Risk & Compliance Manager

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When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Key Accountabilities:

Lead, facilitate and support the risk management process for assigned projects/Partnership/accounts using the available tools.

Lead proactive analysis of key risk indicators and signals across projects and accounts, through Quality Risk Evaluations (QRE), leveraging dashboards, metrics and predictive tools

Serve as a senior consultant on complex consultancy requests and SOP deviations, drawing on deep knowledge of ICH GCP, Parexel processes, regulatory requirements, and applicable country standards

Partner with project teams to sustain an audit/inspection-ready state, providing advanced oversight of storyboards and documentation practices. Assist with audit and inspection preparations, including prioritizing tasks and reviewing critical documents

Serve as the Quality Representative for Quality Event (QE) – Quality Issues and Audit/Inspection Findings

Exemplify adherence to company standards

Mentorship and Team Support

Customer Interactions and Relationship Management

Champion innovative improvement in identifying gaps, leading initiatives, and influencing organizational strategy

Skills:

Knowledge and Experience:

Education:

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