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Senior Regulatory Affairs Associate- Clinical Trial Application

Parexel · Healthcare & Pharma

  • India-Bengaluru-Remote
  • Remote
  • Posted today
  • Healthcare & Life Sciences
Apply on Parexel(opens the employer’s site in a new tab)

About the job

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
Apply on Parexel(opens the employer’s site in a new tab)