Regulatory Affairs Associate (Clinical Trial Application)
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
About Company
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