Associate regulatory Work, Jobs in Arlesey, Hrt (with Salaries)

Senior Regulatory Associate- Fixed Term Contract until 31 August 2027
DLRC —Letchworth
- English
- Microsoft Office
- Analysis skills
Associate - Regulatory
HCR —Cambridge
- Annual leave
- Gym membership
Environmental Advisor
M Group —Stevenage
- £40,000 a year
- Travel
- In-person
- Communication skills
- Annual leave
- Employee assistance programme
8d
Clinical Trial Coordinator
Thermo Fisher Scientific —Cambridge
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- English
Biomedical Associate - Cellular Pathology 12 month FTC
Bedfordshire Hospitals NHS Foundation Trust —Bedford
- £28,392 - £31,157 a year
- Full-time
8d
Clinical Research Associate
TOGL (Holdings) Limited —Cambridge
- Patient monitoring
- In-person
- Communication skills
Quick apply
4d
Retail Sales Advisor - Stevenage
Oak Furnitureland —Stevenage
- £47,035 - £51,788 a year
- Full-time
- Sales
- Retail sales
- Free parking
- Employee assistance programme
Clinical Research Associate
AstraZeneca —Cambridge
- Bachelor's degree
- No degree
- Travel
1d
Deputy Practice Manager
PrimaryCareCareers —Ampthill
- £37,183 - £39,096 a year
- Management
- GP surgery experience
- Leadership
9d
Scientist – Diagnostic Laboratory Sciences (DLS)
Avantor —Cambridge
- Full-time
- Laboratory experience
- Bachelor's degree
- No degree
- Annual leave
SRA, Histology
Flagship Pioneering, Inc. —Cambridge
- Laboratory experience
- Master's degree
- Bachelor's degree
Associate Director, Regulatory Legal Counsel
Illumina —Cambridge
- £110,600 - £166,000 a year
- Full-time
- Management
- English
- Travel
Senior Product Analyst
TJX Europe —Watford
- Full-time
- Bachelor's degree
- APIs
- IT
- Employee discount
Sample Dispatch Technician
Avantor —Stevenage
- Full-time
- Laboratory experience
- No degree
- Communication skills
- Annual leave
Management Associate Commercial
Mundipharma —Cambridge
- Full-time
- Microsoft Excel
- Doctoral degree
- Master's degree
9d
Competence Approval Lead
Kiwa —Dunstable
- Full-time
- Microsoft Powerpoint
- Microsoft Outlook
- IT
- Annual leave
Lab Service Manager
Avantor —Cambridge
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Associate Dentist
H G Dental —High Barnet
- £47,878.59 - £80,000.00 a year
- Part-time
- Bachelor's degree
- Organisational skills
- In-person
Quick apply
5d
Sample Dispatch Manager
Avantor —Stevenage
- Full-time
- Microsoft Excel
- Master's degree
- Bachelor's degree
- Annual leave
Director, Translational Science Lead
GlaxoSmithKline —Stevenage
- £178,200 - £297,000 a year
- Full-time
- Doctoral degree
- Business development
- Leadership
- Annual leave
12d

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Senior Regulatory Associate- Fixed Term Contract until 31 August 2027

DLRC -
Letchworth

Apply Now

Job details

Fixed term contract

Qualifications

English
Microsoft Office
Analysis skills
Project management
Organisational skills
Leadership
Communication skills

Full job description

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 Associate

UK | Hybrid & Flexible Working - Fixed Term Contract until 31 August 2027

We are seeking a Senior Regulatory Associate to support and deliver regulatory projects across UK and EU markets, providing high-quality regulatory support and submissions within a fast-paced consultancy environment.

This role is ideal for a regulatory professional with experience managing regulatory activities across multiple procedures who is looking to further develop their strategic, project management, and client-facing capabilities within a collaborative team.

The opportunity:

You will support the delivery of regulatory projects across a range of products and procedures, preparing and reviewing regulatory submissions, contributing to regulatory strategy, and ensuring projects are delivered compliantly and on time. You will work closely with clients, internal stakeholders, and regulatory authorities while supporting junior colleagues and contributing to business development activities.

Key responsibilities:

Identify, interpret, and apply relevant UK, EU, and US regulations and guidance to support project compliance

Prepare, review, and manage high-quality regulatory submissions with minimal supervision

Review documentation for accuracy, consistency, and completeness

Contribute to regulatory recommendations and SME strategies for client projects

Prepare submissions including CTAs, modifications, MAAs, variations, Scientific Advice requests, PIPs, and Orphan Drug applications

Support regulatory projects, including liaison with regulatory authorities under supervision

Monitor project risks, timelines, and action logs, proactively identifying and escalating issues

Support project planning and stakeholder management to ensure successful project delivery

Assist with budget management and resource planning where applicable

Participate in business development activities including scoping calls, proposal support, and follow-up actions

Analyse regulatory changes and assess their impact on projects and business activities

Mentor junior team members on routine tasks and support knowledge sharing within the team

Ensure all activities are delivered in line with Quality Management requirements and company values.

About you:

Previous hands-on experience in preparation and management of regulatory submissions including CTA submissions in the EU and/or UK and agency interactions. Experience of submissions of other clinical development procedures (PIPs, ODD, Scientific advice) and/or post-marketing activities is advantageous
Good understanding of national and EU regulatory procedures
Ability to contribute to regulatory strategy and interpret relevant legislation, guidance, and procedures
Strong analytical skills with the ability to review complex datasets and identify inconsistencies or risks
Understanding of scientific and regulatory environments
Strong organisational and project management skills, including prioritisation and timeline management
Excellent written and verbal communication skills with the ability to build strong working relationships
Collaborative and team-oriented approach with accountability for individual contributions
Commercial awareness and understanding of consultancy business environments
Ability to mentor and support the development of junior colleagues
Degree in Life Sciences, Pharmacy, or equivalent
Proficient in Microsoft Office applications
Eligible to work in the UK; fluent in English.

Why join us?

We are a consultancy built on integrity, respect, and accountability. Our people are trusted to take ownership, supported to develop, and encouraged to think commercially.

We bring energy and enthusiasm to our work, collaborating closely with clients and partners to deliver practical, sustainable solutions. With flexible working and strong professional development pathways, we offer an environment where regulatory consultants can build influence, capability, and long-term careers.

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.

Apply Now

Refine Your Search

associate regulatory jobs in arlesey, hrt

Senior Regulatory Associate- Fixed Term Contract until 31 August 2027

Associate - Regulatory

Environmental Advisor

Clinical Trial Coordinator

Biomedical Associate - Cellular Pathology 12 month FTC

Clinical Research Associate

Retail Sales Advisor - Stevenage

Clinical Research Associate

Deputy Practice Manager

Scientist – Diagnostic Laboratory Sciences (DLS)

SRA, Histology

Associate Director, Regulatory Legal Counsel

Senior Product Analyst

Sample Dispatch Technician

Management Associate Commercial

Competence Approval Lead

Lab Service Manager

Associate Dentist

Sample Dispatch Manager

Director, Translational Science Lead

I want to receive the latest job alerts for associate regulatory in arlesey, hrt

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