Senior Regulatory Affairs Associate- Clinical Trial Application

Parexel International Pesquisas Clinicas LTDA.

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India-Bengaluru-Remote remote Until 9/1/2026 5+ years exp H-1B sponsor history First posted June 9, 2026 Last posted July 3, 2026
Job 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.

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
About this role

Summary

Manage clinical trial application submissions across regions, ensuring compliance, timeliness, and quality.

Job title

Senior Regulatory Affairs Associate- Clinical Trial Application

Experience level

5+ years

Minimum experience

5+ years exp

Industry

healthcare

Location requirements

Remote work in Bengaluru, India. Remote work allowed.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

project managementregulatory knowledgerisk managementstakeholder engagementcommunication

Preferred skills

None specified

Specializations

clinical trial applicationsregulatory complianceEU CTRglobal submissionsproject management
Locations

Structured locations inferred from the posting.

Bengaluru, Karnataka, India

Remote City