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Regulatory Affairs Specialist ( Labelling)

  1. Mexico
2023-101993
  1. ICON Strategic Solutions (FSP)
  2. Regulatory Affairs

About the role

This vacancy has now expired. Please click here to view live vacancies.

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.


What you will be doing:

  • A Regulatory Specialist is a Regulatory professional who contributes to drug development, through provision of regulatory guidance and operational support to early drug development, agency interactions, clinical trial applications, marketing application and post approval support.

    Regulatory advice to drug development is key to ensuring our clients pursue first time right strategies to overall product development and to clinical programme development.


You are:

  • Scientific (any science discipline)or Pharmacy degree
  • Regulatory specialist could come from any ICON department (especially ICO, Clin ops) if you have prior regulatory experience in Agency, CRO or Pharma Industry or from the role of SSUA & labelling.
  •  English fluent ,write & read 



Why ICON?

Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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The Role of Regulatory Affairs in Clinical Research

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Industry

Content type

Blogs

Publish date

01/18/2024

Summary

Introduction to Regulatory Affairs in Clinical Research Regulatory affairs play a pivotal role in ensuring the safety, efficacy, and quality of pharmaceutical products and medical devices. I

Teaser label

Explore the pivotal role of regulatory affairs in clinical research with our insightful blog.

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