Senior Regulatory Affairs Associate

parexelΒ· 1785 Parexel International India safety services Private Limited
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🌍 RemoteπŸ“ India-Bengaluru-RemoteFull time

About this role

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

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:

  • Bachelor’s 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

Frequently Asked Questions

Is the salary disclosed for the Senior Regulatory Affairs Associate position at parexel?
The salary for this Senior Regulatory Affairs Associate role at parexel is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Is the Senior Regulatory Affairs Associate job at parexel remote?
Yes, this Senior Regulatory Affairs Associate position at parexel is remote, with team members based in India-Bengaluru-Remote. You can work from home or anywhere in the supported regions.
Is the Senior Regulatory Affairs Associate role at parexel full-time or part-time?
This is listed as a Full time position. It is posted as a Senior Regulatory Affairs Associate role in the 1785 Parexel International India safety services Private Limited department at parexel.
Which team or department does the Senior Regulatory Affairs Associate at parexel belong to?
This Senior Regulatory Affairs Associate position is part of the 1785 Parexel International India safety services Private Limited department at parexel. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Senior Regulatory Affairs Associate position at parexel?
Click the "Apply Now" button on this page. You will be redirected to parexel's official application portal hosted on workday where you can submit your application directly.
When was the Senior Regulatory Affairs Associate job at parexel posted?
This Senior Regulatory Affairs Associate position at parexel was posted on Sep 9, 2026. Apply as soon as possible β€” early applications are often reviewed first.
Senior Regulatory Affairs Associate
parexel
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You'll be redirected to parexel's official application page on Workday.