Parexel hiring Regulatory Affairs Associate Consulting Job openings. Interested & Eligible Candidates Apply Now. Work from Home option available for all selected Candidates

Job type : Full time

Work location : work from home

Job Description

Around 2 to 5 relevant experience in authoring standard operating procedures for various types of regulatory submissions including initial submissions, product post approval compliance activities and other license maintenance activities

Working knowledge of EU/US 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

Good understanding of regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions as well as knowledge of global pharmaceutical legislation and guidance specifically linked to regulatory CMC aspects in the ICH countries.

Prior working experience in Regulatory Information Management Systems like Veeva Vault would be desirable

Strong communications skills

Ability to work independently with minimum supervision

Recruitment Process : Interested & Eligible Candidates Apply by clicking below Link

Parexel Work from home jobs

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