About this role
Regulatory Consultant at Syneoshealth. Location: India or Gurugram. Role: preparing submissions, managing activities, conducting research Requirements: Require 4+ years regulatory affairs experience, MPharm/Masters level education, CMC module 3 and post-approval variation authoring, EU/GCC market experience, and experience preparing IND/PMA/NDA/MAA/CTD electronic submissions. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Office Commitment: Full Time Workplace: Remote Languages: English