Senior Regulatory Affairs Associate- Clinical Trial Application
Job Summary
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds 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 were committed to making a difference.
The Clinical Trial Submission Lead (CTSL) is responsible for end-to-end planning coordination and execution of Clinical Trial Applications (CTA) across EU CTR and Rest of the World (ROW) regions. This role ensures timely high-quality and compliant submissions through effective cross-functional collaboration proactive risk management and strong regulatory expertise.
Key Responsibilities:
- Lead end-to-end CTA project management across multiple studies and countries
- Plan track and deliver submissions aligned with timelines and regulatory requirements
- Manage risks dependencies and complexities in global regulatory environments
- Apply knowledge of EU CTR and ROW CTA requirements
- Manage core clinical and regulatory documentation
- Collaborate with cross-functional global teams
- Build and maintain stakeholder relationships and resolve conflicts
- Monitor KPIs related to timelines and deliverable quality
- Identify risks and lead quality investigations as needed
Qualifications & Experience:
- Bachelors degree in Life Sciences Pharmacy or related field
- Minimum 5 years of industry experience in pharmaceutical CRO or similar
- Experience in Clinical Trial Application submissions (EU CTR & ROW)
- Strong project management experience in a global/matrix environment
- Familiarity with clinical trials and regulatory processes
Key Skills:
- Project Management & Execution
- Regulatory Knowledge (EU CTR & Global Submissions)
- Risk & Issue Management
- Stakeholder Engagement
- Strong communication and problem-solving skills
- Adaptability resilience and teamwork
Required Experience:
Senior IC
About Company
Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more