Established in 2005, the DLRC Group has developed a deserved reputation for being a leading consultancy, with a wealth of regulatory and scientific knowledge and considerable experience in both leadership and management. The company has recently expanded to include affiliates based in Germany and the US.
Our growing team comprises over 90 qualified professionals with a pharmaceutical and/or regulatory background, as well as over 30 dedicated supporting staff in areas of Business Development, Finance, Business Services and People Practices. We provide services to over 130 organisations, enabling them to achieve their strategic and operational development objectives.
DLRC’s expertise and flexible working approach ensures the provision of a highly motivated team who interact effectively with clients and regulators globally, to support both single issues and long-term commitment to projects.
Senior Regulatory Consultant – Permanent Opportunity
UK | Hybrid & Flexible Working
We are seeking a Senior Regulatory Consultant to lead complex regulatory programmes and deliver strategic, high-value advice to clients across UK, EU, and US markets.
This is a senior, client-facing role for an experienced regulatory professional who thrives on complexity, leadership, and influence — and who wants to shape both regulatory strategy and business growth within a values-led consultancy.
The opportunity:
You will take ownership of major regulatory engagements, define and defend regulatory strategy for complex products, and oversee high-quality submissions across global frameworks. Working closely with clients and regulatory authorities, you will provide clear, confident leadership while mentoring teams and contributing to the firm’s continued growth.
Key responsibilities:
* Lead major regulatory programmes and act as a senior subject matter expert
* Develop, defend, and deliver robust regulatory strategies across UK, EU, and US frameworks
* Oversee complex submissions including CTAs, MAAs, variations, Scientific Advice, PIPs, and Orphan Drug applications
* Manage regulatory procedures and direct interactions with health authorities
* Interpret complex datasets and evolving regulatory environments
* Provide oversight of resourcing, budgets, risk, and change control
* Build and maintain senior client relationships and identify growth opportunities
* Mentor and develop regulatory professionals
* Contribute to business development, marketing, and conference activity
* Ensure delivery in line with Quality Management and best practice.
About you:
* Extensive experience in regulatory affairs, including leadership of major projects
* Proven ability to shape and defend complex regulatory strategies
* Strong experience with global submissions and agency engagement
* Deep understanding of EU, national, and US regulatory frameworks
* Confident communicator and negotiator at senior stakeholder level
* Commercially astute, with experience supporting business development
* Degree in Life Sciences, Pharmacy, or equivalent
* Eligible to work in the UK; fluent in English
We are a consultancy defined by integrity, respect, and accountability. Our people are trusted to lead, encouraged to think boldly, and supported to deliver exceptional outcomes.
We combine energy and ambition with a collaborative mindset, turning complex challenges into sustainable, transformative solutions. Through flexible working, unrivalled professional development, and strong internal and external partnerships, we create an environment where senior professionals can grow, influence, and make a lasting impact.
We review applications and conduct interviews on a rolling basis, so don’t delay in applying. Our Talent Acquisition team will be in touch with an update once your application has been reviewed.
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