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Principal Consultant

United Kingdom - Any Region - Home Based Date posted 02/11/2021 Job ID 64190BR

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.

In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.

Success Profile

Check out the top traits we're looking for and see if you have the right mix.

  • Detail-Oriented
  • Proactive
  • Problem-Solver
  • Results-Driven
  • Organized
  • Multi-Tasker
  • "When submitting major market applications, it’s key to ensure that the technical integrity of all data meets regulated requirement standards. Parexel makes this possible with a diverse team of seasoned professionals who care about getting important medicines to patients. This is Regulatory Operations at its best."

    Chris – Associate Director, Regulatory & Access
  • "In this role, I have had the unique opportunity to work with regulatory experts who are not only some of the most distinguished in their field, but are also some of the most compassionate people I know. I’ve been able to grow so much professionally by standing on the shoulders of giants!"

    Riley – Regulatory Affairs Consultant

Rewards

  • Global Impact

    We are one truly global team working together to propel each client´s journey ahead faster.

  • Balance

    We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

  • Collaboration

    Work with industry leaders and subject matter experts.

  • Freedom

    The ability to innovate, ask “what if” and try new solutions without fear of failure.

  • Variety

    Opportunities to work on multiple accounts – never boring!

  • Management

    Strong management with depth of experience working for global health authorities.

Responsibilities

We are recruiting for a Principal Consultant of Regulatory Affairs, to be home-based in Europe. Experience in Clinical regulatory SME, and experience in numerous therapeutic areas including paediatrics is highly desirable.

Experience Required
  • High-level consulting skills
  • Critical thinking and problem-solving skills
  • Project leadership and management knowledge
  • Excellent interpersonal and intercultural communication skills, both written and verbal
  • Client-focused approach to work
  • Results orientation
  • Teamwork and collaboration skills
  • Proficiency in local language and extensive working knowledge of the English language
  • Account planning and support
  • Networking
  • Business acumen and analysis
  • Self-confidence and control

Qualifications

Experience required:

Numerous years of experience with expert level industry or regulatory knowledge; experience with a regulatory agency (such as FDA, MHRA) is a plus.

Minimum of a Bachelor’s Degree in a Scientific or Technical Discipline, PhD or other advanced degree (i.e. MBA) preferred

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