Clinical research associates & coordinators Work, Jobs in Dunsfold, Sry (with Salaries)

CDC Trial Manager I
Novo Nordisk —Gatwick Airport
- Computer literacy
- English
- No degree
7d
Research Facilitator
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
- £29,812 - £32,715 a year
- Full-time
- Free parking
11d
Data Curator
ICR —Sutton
- £31,445 - £33,600 a year
- Hybrid work
- SQL
- Linux
- Communication skills
7d
Clinical Research Associate II (French speaking)
Ergomed —Guildford
- Full-time
- Remote
- English
- Bachelor's degree
- Travel
Quick apply
10h
Clinical Research Senior Administrator
The Royal Marsden NHS Foundation Trust —Sutton
- £36,943 - £44,900 a year
- Full-time
7h
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Senior Trial Manager - Lung and Mesothelioma Research
The Royal Marsden NHS Foundation Trust —Sutton
- £55,524 - £62,652 a year
- Full-time
6d

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Research Facilitator
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
They will assist the Research Governance Lead with study setup, engaging with sponsors, clinicians, support departments and managers to ensure that research…
£29,812 - £32,715 a year
11d
Senior Clinical Trials Facilitator - Study Set up Specialist
Guy's and St Thomas' NHS Foundation Trust —London
Engage with EPIC (Electronic Patient Records) and facilitate building site level electronic prescription platform: submit key documents relevant for EPIC drug…
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CDC Trial Manager I

Novo Nordisk -
Gatwick Airport

Apply Now

Job details

7 days ago

Qualifications

Computer literacy
English
IT
Communication skills

Full job description

CDC Trial Manager I

Category: Clinical Development

Location: Gatwick, South East, GB

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.

Your new role

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

Leading the CDC project team (CRAs and CTAs and other relevant roles), planning and conducting trial team meetings, and co-monitoring based on project risks

Managing the country budget, driving study start-up in collaboration with the study start-up unit, and overseeing clinical supplies processes including import and local depot set-up

Consolidating CDC input on key trial documents, systems and vendors (e.g. CRF, diary), and keeping CTMS updated at trial country level

Monitoring recruitment and retention, reviewing and approving monitoring visit reports and protocol deviations, and ensuring data cleaning and DBL deliverables per the Data Flow Plan

Coordinating communication between Trial Squads, CRAs and local/regional stakeholders, escalating risks proactively and supporting issue resolution with trial vendors

Planning and executing local Investigator and Monitor meetings, and supporting global equivalents where required

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

Your new department

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:

A Life Science degree or equivalent qualification

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

Strong project and resource management skills, with the ability to drive deliverables forward across a complex stakeholder landscape

Excellent knowledge of clinical trial methodology and up-to-date understanding of the clinical trials environment across Europe – ICH-GCP, regulatory requirements and SOPs – along with a solid grasp of the drug development process (current GCP training and certification required)

Computer literacy and IT proficiency, including CTMS, EDC and Veeva Vault;

Excellent communication and interpersonal skills in English, with the diplomacy and self-drive to influence, align and inspire teams both locally and globally

Working at Novo Nordisk

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.

What we offer

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.

Deadline

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.

Apply Now

Refine Your Search

clinical research associates & coordinators jobs in dunsfold, sry

CDC Trial Manager I

Research Facilitator

Data Curator

Clinical Research Associate II (French speaking)

Clinical Research Senior Administrator

Sr. Clinical Project Manager (Europe)

Senior Clinical Programmer I

Senior Trial Manager - Lung and Mesothelioma Research

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