Clinical Development Centre (CDC)
United Kingdom
Shape the future of clinical research in the UK – and see your work translate into better outcomes for patients living with serious chronic diseases.
As Trial Manager I, you will lead the delivery of clinical trials in the UK from site selection through to database lock and archiving, ensuring every study runs in line with the protocol, ICH-GCP, UK legislation and Novo Nordisk SOPs. You will be the driving force behind your trials, connecting global Trial Squads with local CRAs and CTAs to bring new therapies one step closer to patients.
Day-to-day, your responsibilities will include:
Acting as project manager for assigned clinical trials within the CDC – owning strategy, feasibility, recruitment, retention, risk management, database lock and archiving
Consolidating CDC input on key trial documents, systems and vendors (e.g. CRF, diary), and keeping CTMS updated at trial country level
Ensuring full compliance with ICH-GCP, the ABPI Code of Practice, Novo Nordisk Business Ethics, quality standards and your Personal Compliance Plan, and facilitating audits and inspections as required
As part of Global Trial Portfolio (GTP) you will join one of our largest operational units. With a promise to outperform the competition, we continue to be the growth driver for Novo Nordisk, and to improve health at scale across the globe.
Within GTP, you will join the UK Clinical Development Centre (CDC) – the team responsible for delivering Novo Nordisk's clinical trial portfolio in the UK. We work in close partnership with global Trial Squads, local CRAs, investigators and sites to ensure trials are executed to the highest quality, on time and in full compliance. Here, your work will directly shape the evidence that brings new treatments to patients.
Your skills & qualifications
We are looking for an experienced clinical trials professional – potentially a senior CRA ready to step up into trial management – who thrives on ownership, coordination and delivery in a highly regulated environment. To succeed in this role, you will bring:
Proven experience managing clinical trials, ideally including multi-centre studies; experience as a senior CRA looking to take the next step into trial management is highly relevant, and international trial co-ordination or exposure to more than one phase of development is a plus
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.
There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.
2 August 2026. (Applications are reviewed on an ongoing basis).
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
