Regulatory Affairs Associate

 Posted 2 hours ago
  
 India
  
2-5 years experience
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AI Summary

The role is responsible for the end-to-end planning, coordination, and execution of Clinical Trial Applications across EU CTR and Rest of the World regions. This includes managing project timelines, regulatory documentation, and collaborating with cross-functional global teams to ensure compliant submissions.

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 3+ 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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