Regulatory specialist Work, Jobs in Ardingly, Wsx (with Salaries)

Study Start Up Specialist
Novo Nordisk —Gatwick Airport
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
2d
Behaviour Analyst
The Quest School —Paddock Wood
- £34,000 - £45,000 a year
- Full-time
- English
- Master's degree
- In-person
- Free parking
- Health & wellbeing programme
Quick apply
Associate Compliance Auditor
Collinson —Haywards Heath
- Hybrid work
- Microsoft Office
- Hotel
- Analysis skills
Specialist HR Lead
Anderida Adolescent Care —Eastbourne
- £50,000 - £65,000 a year
- Full-time
- Management
- Microsoft Office
- Driving
- Annual leave
- Sick pay
Quick apply
6d
Assistive Technology Manager
Chailey Heritage Foundation —Lewes
- £42,000 - £49,000 a year
- Full-time
- Rehabilitation centre
- Communication skills
- Employee assistance programme
8d
Emergency Planning Officer
Sussex Community NHS Foundation Trust —Brighton
- £39,959 - £48,117 a year
- Part-time
1d
Stores Advisor
Sureserve —Horsham
- £23,000 - £26,000 a year
- Microsoft Word
- Microsoft Outlook
- Computer literacy
- Annual leave
- Employee assistance programme
Quick apply
Reward and Wellbeing Manager
Brainkind —Burgess Hill
- £45,000 - £55,000 a year
- Full-time
- Free parking
- Annual leave
Compliance Manager
Adams and Remers —Lewes
- £45,000 - £55,000 a year
- Full-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
- Health & wellbeing programme
- Employee discount
Quick apply
Assistant Director of Mental Health & Autism
Active Prospects —Reigate
- £75,000 a year
- Full-time
- Hybrid work
- Management
- Employee assistance programme
Quick apply
1d
Quality Assurance and Compliance Monitoring Officer
CAE Inc. —Burgess Hill
- Travel
- Communication skills
Access Arrangements Coordinator (Part-Time)
Our Lady of Sion School —Worthing
- £9,960 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Quick apply
Occupational Therapist
East Sussex County Council —Lewes
- Full-time
- Communication skills
Aircraft Interior Specialist
JMC Aviation —Biggin Hill
- Communication skills
- Mechanical knowledge
- Relocation assistance
- Annual leave
Flight Simulator Instructor Trainer (Train-the Trainer)
CAE Inc. —Burgess Hill
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Analysis skills
Clinical Development Nurse - South West
Barchester Healthcare —Henfield
- £55,000 a year
- Travel
- Leadership
- Referral programme
Quick apply
Distribution Retentions Specialist
OneFamily —Brighton
- Full-time
- Microsoft Excel
- Microsoft Office
Managing Director, Agentis Pharmacy
Ashtons Hospital Pharmacy Services Limited —Brighton
- Full-time
- Master's degree
- Business
- Health & wellbeing programme
Quick apply
Freshdesk coordinator
Inspiration Healthcare Ltd —London
- Full-time
- Hybrid work
- Customer service
- Microsoft Office
- Administrative experience
Quick apply
12d
Operations Integrator (Airfield)
Gatwick Airport Limited —Gatwick Airport
- £56,000 a year
- Driving
- Communication skills
- Free parking
- Employee discount
3d

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Study Start Up Specialist

Novo Nordisk -
Gatwick Airport

Apply Now

Job details

2 days ago

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Computer literacy
Microsoft Office
Administrative experience
IT

Full job description

Study Start Up Specialist

Category: Clinical Development

Location: Gatwick, South East, GB

Start Up Specialist

Help bring new clinical trials to life in the UK – and play a vital role in getting life-changing treatments to the patients who need them. If you thrive on detail, regulation and making things happen, this is your moment.

Your new role

As our new Start Up Specialist, you will be responsible for delivering regulatory, ethics and national approvals for clinical trials managed by our Clinical Development Centre UK (CDC UK). Working in close partnership with the Start Up Trial Manager and the wider Trial Squad, you will negotiate and maintain site contracts, secure site approvals, and ensure timely site activation – all in line with UK regulations, ICH GCP and Novo Nordisk's quality standards.

Your day-to-day responsibilities will include:

Preparing and submitting UK nation (HRA and devolved nation), MHRA and Research Ethics Committee (REC) approvals across the trial lifecycle, acting as submission lead via systems such as IRAS, and booking REC meetings as required
Handling regulatory lifecycle requirements of clinical trial authorisations and securing local secondary care, primary care and Patient Identification Centre (PIC) approvals
Supporting preparation of the Clinical Trial Agreement (mCTA), leading cost negotiations with R&D offices at Trusts/Boards and GP sites, and arranging full execution of contracts
Coordinating amendments for ongoing trials with the CDC Trial Manager and providing 'Green-light' and submission documentation to Trial Managers and Clinical Trial Assistants within agreed timelines
Providing trial site status updates to the Trial Squad, and reviewing and approving clinical trial labels in line with UK regulatory requirements
Ensuring compliance with UK legislation, the national governance framework, EU directives where applicable, ICH GCP and Novo Nordisk SOPs – including sTMF oversight, filing and archiving
Contributing to ongoing process improvement by interpreting and standardising new approvals processes and communicating changes to relevant stakeholders

Your new department

As part of International Operations, you will join our largest operational unit. Covering 194 countries and 95% of the world's population, more than 18,000 of us work passionately to serve 35 million patients each day. 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 International Operations sits Clinical Development Centre UK (CDC UK), the team responsible for delivering high-quality clinical trials across the UK. We work in close-knit Trial Squads where Start Up Specialists, Trial Managers, CRAs and Clinical Trial Assistants collaborate to bring new studies to life – navigating an evolving approvals landscape and ensuring patients in the UK can access tomorrow's treatments today.

Your skills & qualifications

We are looking for a highly organised, detail-oriented professional who enjoys working across a variety of stakeholders in a fast-changing regulatory environment. To succeed in this role, you will bring with you:

Some experience working in an administrative role within the pharmaceutical or healthcare environment; a degree or equivalent qualification is desirable
Good knowledge of clinical trial methodology and an up-to-date understanding of the UK clinical trials environment – including ICH GCP, regulatory and ethics requirements and SOPs – with a valid GCP training certificate
Hands-on experience using internal and external IT systems such as IRAS, docusign, Veeva, alongside strong computer literacy and proficiency in Microsoft Office (Word, Excel, PowerPoint)

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

25 June 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

regulatory specialist jobs in ardingly, wsx

Study Start Up Specialist

Behaviour Analyst

Associate Compliance Auditor

Specialist HR Lead

Assistive Technology Manager

Emergency Planning Officer

Stores Advisor

Reward and Wellbeing Manager

Compliance Manager

Assistant Director of Mental Health & Autism

Quality Assurance and Compliance Monitoring Officer

Access Arrangements Coordinator (Part-Time)

Occupational Therapist

Aircraft Interior Specialist

Flight Simulator Instructor Trainer (Train-the Trainer)

Clinical Development Nurse - South West

Distribution Retentions Specialist

Managing Director, Agentis Pharmacy

Freshdesk coordinator

Operations Integrator (Airfield)

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