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Senior Regulatory Affairs Associate- Clinical Trial Application

Key Facts

Remote From: 
Full time
Senior (5-10 years)
English

Other Skills

  • Communication
  • Problem Solving
  • Adaptability
  • Resilience
  • Teamwork

Roles & Responsibilities

  • 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

Requirements:

  • 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
  • Collaborate with cross-functional global teams

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

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