Regulatory Affairs Consultant with Portuguese
We are seeking a person who will:
Contact details
Various opportunities for professional and personal growth
Work with industry leaders and subject matter experts
Strong management with depth of experience working for global health authorities
Main requirements:
Minimum of a Bachelor’s Degree in a Scientific or Technical Discipline, Advanced Degree.
Several years of experience in an industry-related environment (CRO/Pharma).
Experience with Marketing Authorization application.
Fluent vocal and written Portuguese and English.
Benefits:
On your PAREXEL journey, we support you with leading-edge technology, highest caliber team members, and a manager who know your strengths. We are here to listen and help you move forward with your individual career path.
Madrid, Spain
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Prepare / supervise submission of documents, fill out initial application forms and check the quality of submission packages.
Prepare label designs for the investigational medicinal products.
Monitor changes on the ongoing basis in EU legislation, advising on EU guidelines, EU requirements.
Act in compliance with EU's pharmaceutical law, ICH-GCP, EU directives and in line with local and global procedures.
By being hired into one of our positions within PAREXEL Consulting, you’ll be a key member of the PAREXEL International team. Our regulatory professionals come from a variety of backgrounds, and your experience will add to the broad assortment of knowledge and skills that serve every area of our business.
Embrace being a part of an innovative leading organization in the life sciences industry
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