Dedicate your Consulting expertise towards improving the world's health

Become a part of a team that comes to work each day to help make a difference.

Our focus never waivers from the patients waiting for a product and so we have brought together the best minds. Help our clients chart the best, most-efficient, course through global regulatory, market access, and commercial hurdles.

Parexel’s Regulatory & Access consulting organization includes ~100 former regulators and HTA assessors. Because they wrote the guidance yesterday, we know exactly how to interpret it today.

Our strategic advisory teams help companies to establish a systematic integration of regulatory requirements, patient engagement, and pricing and market access into the R&D process for better, faster drug development. Because ‘the old way’ just isn’t financially sustainable or effective today.

Regulatory Consulting

Our regulatory experts work with a deep understanding of intricate regulatory requirements. Many of them are former regulators themselves, leveraging their strategic regulatory and therapeutic insights to enhance and optimize development. We add value with our early engagement, global development plans, common core dossiers, and patient-focused outcomes. Help companies prioritize which products to develop in which patients through which targets for the best response we can get.

Access Consulting

Our access experts optimize pricing and secure reimbursement with minimum restrictions, for the full indication population, and with minimum delay. We address the questions our clients must answer to secure optimal market access. What is the value of the compound, how can it be maximized, what evidence is needed, and how can we generate it? Support commercialization as well as bringing commercial issues and insights into the development phase.

What makes our roles different?

Impact

• Strategize with emerging and big pharma clients to move beyond enforcing guidance and find solutions.
• Build long term relationships with our clients.
• Work on a variety of cutting edge products.
  • Precision medicine therapies that represent the evolution of patient care.

Growth

• Get to work with an incredibly talented team of global regulatory professionals with an unmatched depth of experience.
• Use your expertise, stretch your thinking, and continue to learn in a respectful and collaborative atmosphere.
• Broaden your outlook of the drug development process. Exposure to several therapeutic areas and clients.

Related Content

Mollie Quinn - Director, Regulatory & Access

She shares her career progression, the flexibility to truly work from anywhere, the insights she is gaining from participating in Parexel's Women in Leadership program, and what “We care” means to her.

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