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Senior Regulatory Affairs Associate- Clinical Trial Application

Parexel


Job Location:

Bengaluru - India

Monthly Salary: Not provided by the employer
Posted: 11 June 2026 (30+ days ago)
Application Deadline: 8 September 2026
Vacancies: 1 Vacancy
The job posting is outdated and position may be filled

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.

Job Summary:

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

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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

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