Regulatory Affairs Associate (Clinical Trial Application)

Parexel

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profile Job Location:

Bengaluru - India

profile Monthly Salary: Not Disclosed
Posted on: 21 hours ago
Vacancies: 1 Vacancy

Job Summary

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds 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 were committed to making a difference.

  • 2-4 yrs yrs in-depth knowledge of Indian regulatory guidelines for clinical trials including NDCT Rules.
  • Hands-on experience with SUGAM portal for Initial Clinical Trial Application (CTA/iCTA) submissions and amendments.
  • Ability to liaise effectively with global sponsors and cross-functional teams.
  • Prepare necessary documentation presentations and briefing materials for SEC meetings
  • Strong understanding of global regulatory expectations and harmonization with Indian requirements.
  • Acquired hands-on expertise in managing and completing clinical trial registrations on the Clinical Trials Registry-India (CTRI) portal.
  • Updated with current Guidelines and Gazette Notifications to give suggestions/comments to respective Regulatory authorities and Govt. regulatory bodies.
  • Working knowledge of India regulatory procedures including adaptability to strict Health Authority and Sponsor timelines for completing submissions
  • Manage timelines for query responses and ensure on-time submission through SUGAM portal or other regulatory platforms.
  • Clear oral and written communication skills
  • Acceptability towards varied cultural mindsets to collaborate efficiently with client counterparts and other internal stakeholders as well
  • Execute and maintain submission delivery plans submission content plans and proactively provide status updates to designated stakeholders.
  • Strong communications skills and ability to guide and mentor team members.
  • Ability to work in different time zones
  • Ability to work independently


Required Experience:

IC

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds 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...
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About Company

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Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more

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