Senior Manager, Regulatory Affairs
parexel
| Company | parexel |
| Category | Legal & Compliance |
| Location | 2 Locations |
| Remote | — |
| Employment | Not stated |
| Level | Manager |
| Salary | Not stated by the employer |
| Posted | 24 Jul 2026 |
| Last verified | 11 Aug 2026 |
| Source | Employer ATS (workday) |
Description
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.
A Senior Manager within R&A provides leadership and direction to consultants, senior consultants and managers, actively managing employee performance and development. A Senior Manager acts as a role model and provides a broad range of consulting services and may be responsible for a specific function/technical area.
Key Responsibilities
• Extensive experience in Regulatory Affairs, including expertise in EU Clinical Trials Regulation (EU CTR) and experience leading and developing teams.
• Act as the Subject Matter Expert (SME) for the EU Clinical Trials Regulation (EU CTR), providing strategic regulatory guidance and ensuring compliant implementation.
• Drive capability building within the team through coaching, mentoring, training, and knowledge-sharing initiatives.
• Contribute to organizational EU CTR-related projects, process improvements, and strategic initiatives.
• Support the development, review, and maintenance of functional Standard Operating Procedures (SOPs).
• Provide support during regulatory audits and inspections.
• Deliver regulatory consultancy and client-focused guidance, fostering strong stakeholder partnerships.
• Lead and manage a team, ensuring performance, development, and operational excellence.
Skills and Competencies
• Strong expertise in EU Clinical Trials Regulation (EU CTR) and associated regulatory requirements.
• Ability to interpret regulatory intelligence, assess impact, and translate requirements into practical processes and implementation plans.
• Solid understanding of regulatory operations, workflows, and compliance standards.
• Excellent stakeholder management and communication skills, with experience collaborating across global teams and clients.
• Strong analytical, problem-solving, decision-making, and risk mitigation capabilities in a dynamic environment.
• Demonstrated ability to work collaboratively and influence cross-functional teams in a consultative manner.