Jobs Companies Parexel Senior Regulatory Affairs Associate

À propos de ce poste Senior Regulatory Affairs Associate chez Parexel

Parexel · Télétravail · India-Bengaluru-Remote

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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À propos de Parexel

Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies a

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