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Parexel

Regulatory Affairs Consultant

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  • Posted 13 days ago
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Job Description

  • Around 7-10 years of relevant experience in handling life cycle management (LCM) of approved/marketed drug products (Biologicals, Vaccines, ) in various markets, mainly in US, EU, Japan, Canada Switzerland, Australia.
  • Good understanding of regulatory framework, including regional trends, for various types of applications and procedures.
  • Lead and / or contribute to the planning, preparation, authoring and delivery of regulatory maintenance submissions from either a global and/or regional perspective.
  • Working knowledge of US, EU, Japan, Canada, Switzerland, Australia regulatory procedures including post approval requirements. Knowledge of ROW markets regulatory legislations would be an added advantage
  • Experience in handling CMC related health authority queries, and author responses to HA requests
  • Preparation / Review of Regulatory gap analysis and strategy documents (with remediation plans for identified gaps) for submissions like IND, IMPD, DMF, BLA, NDA, and MAA applications.
  • Authoring and review of CMC component of Marketing Authorization Applications & Variations for various types of medicinal products (orals & parenteral) for filing in EU through different types of procedures (DCP/MRP/National Procedures).
  • Authoring CMC component for marketed products, of Annual Reports, Variations, expansions, site transfers, Renewals in EU (Type IA/IB/II/IAIN), and US, Canada, Switzerland and RoW markets.
  • Evaluation of change controls and deviations and identification of required documentation and strategy for US, EU, Japan, Canada, Switzerland, Australia submissions and other markets.
  • Co-ordination with internal and external stakeholders for documentation required for various submissions. Identify quality and/or timeliness issues with source documents, as early as possible.
  • Develop up-to-date knowledge about regulatory guideline updates and applying regulatory requirements and their impact on submissions.
  • Working experience in Regulatory Information Management Systems (RIMS) like Veeva Vault.
  • Strong communications skills and ability to guide and mentor team members.
  • Ability to work independently.

Knowledge And Experience

  • Several years of experience in an industry-related environment

Education

  • Minimum of a Bachelor's Degree in a Scientific or Technical Discipline, Advanced Degree Preferred

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About Company

Job ID: 144665159

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