Regulatory Affairs - Talent Pool

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Full Remote
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Offer summary

Qualifications:

University-level education in Life Sciences, Previous experience in regulatory affairs (level-dependent), Strong team spirit, flexibility, accountability, and organizational skills, Fluency in English (written and spoken).

Key responsabilities:

  • Ensure regulatory submissions and activities adhere to global health authority guidelines
  • Develop and execute regulatory strategies
  • Collaborate with cross-functional teams to drive project success
  • Maintain client relationships and deliver high-quality consultancy services

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Parexel XLarge http://www.parexel.com
10001 Employees
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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Join Parexel's Regulatory Affairs Team: Shape the Future of Healthcare

Parexel, a leading Clinical Research Organization, is seeking talented professionals at all levels to join our dynamic Regulatory Affairs and Operations team. We are looking for Associates, Consultants, and Senior Experts who are passionate about ensuring regulatory success in the ever-evolving pharmaceutical and biotechnology landscape.

Who We Are: At Parexel, our Regulatory Affairs team is at the forefront of global healthcare innovation. We work closely with health authorities worldwide, including the US-FDA, EMA, and NMPA, to develop unique regulatory strategies, secure submission approvals, and maintain compliance for trials and products across diverse therapeutic areas.

What We Offer:

  • Exposure to cutting-edge projects in Orphan Drug, Rare Disease, OTC Drug, Cell and Gene Therapies (C&GT), and more

  • Opportunity to work with global teams and clients

  • Career growth across various levels from Associate to Senior Consultant

  • Continuous learning and development in a rapidly evolving field

  • Possibility to work from home

Key Responsibilities Across Levels:

  • Ensure regulatory submissions and activities adhere to global health authority guidelines

  • Develop and execute regulatory strategies

  • Collaborate with cross-functional teams to drive project success

  • Maintain client relationships and deliver high-quality consultancy services

  • Stay updated on regulatory trends and contribute to process improvements

Requirements:

  • University-level education in Life Sciences

  • Previous experience in regulatory affairs (level-dependent)

  • Strong team spirit, flexibility, accountability, and organizational skills

  • Fluency in English (written and spoken)

  • Desire to grow in a fast-paced, innovative environment

Register your interest at Parexel and be part of a team that's shaping the future of healthcare through regulatory excellence. Whether you are starting your career or bringing years of expertise, we hope we can find a place for you to thrive and make a difference.

Required profile

Experience

Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Organizational Skills
  • Accountability
  • Physical Flexibility
  • Team Motivation

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