Regulatory affairs specialist Work, Jobs in Staines Upon Thames, Sry (with Salaries)

Regulatory Affairs Specialist
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Communication skills
- Employee assistance programme
1d
Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK
Cepheid —Amersham
- Full-time
- Remote
- Master's degree
- Bachelor's degree
- Annual leave
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Sr. Specialist, Regulatory Affairs
The Bountiful Company —Tring
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Nutrition Specialist (Global Regulatory & Corporate Affairs)
Oatly AB —London
- Part-time
- Hybrid work
- English
- Master's degree
- Travel
Quick apply
Medical Information Specialist - US Hours
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Senior Regulatory Specialist
Androlabs —London
- £85,000 - £108,000 a year
- Full-time
- Hybrid work
- IT
- Annual leave
Quick apply
Expert Consultant – Healthcare | Safety, Risk & Regulatory
Boston Consulting Group —London
- Full-time
- Doctoral degree
- Master's degree
- Business development
13h
Senior Manager – ESG and Sustainability Regulatory Legal
Pwc UK —London
- Full-time
- Hybrid work
- Analysis skills
- Presentation skills
Director - Regulatory Affairs Lifecycle Management Non-Medicines
Perrigo —London
- Hybrid work
- Bachelor's degree
- In-person
- Leadership
Medical Information Specialist - Afterhours
EVERSANA —London
- Weekend availability
- Remote
- Microsoft Word
- Microsoft Excel
- English
Quick apply
4d
Account Executive - Agricultural Regulatory Intelligence
FoodChain ID Group, Inc —London
- Full-time
- Remote
- Sales
- Salesforce
- English
10d
Regulatory Engagement & Advocacy Manager – UK and France
Nadara —London
- Full-time
- Analysis skills
- Communication skills
Medical Information Specialist - German & English speaking
EVERSANA —London
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
Quick apply
Analyst - Regulatory Market Access and Compliance
Access Partnership —London
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Analyst
Access Partnership —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
South & EE Team Regulatory Affairs Lead
Shell Energy —London
- Full-time
- Engineering
- English
- Supervising experience
Specialist, Quality Audits - Biosimilars
Advanz Pharma —London
- Travel
- APIs
- Employee assistance programme
4d
Director - Regulatory Affairs Lifecycle Management Medicines
Perrigo —London
- Hybrid work
- Bachelor's degree
- In-person
- Leadership
UK & Europe Corporate Communications Lead
TransUnion —London
- Full-time
- Marketing
- Project management
- Employee stock purchase plan
- Annual leave

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regulatory affairs specialist jobs near staines upon thames, sry

Regulatory Affairs Specialist

ICON Plc -
Reading

Apply Now

Job details

Full-time
1 day ago

Benefits

Company pension
Employee assistance programme

Qualifications

Bachelor's degree
Communication skills

Full job description

Regulatory Affairs Specialist

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Regulatory Affairs Specialist at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your role will involve delivering regulatory affairs work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

Undertaking variable duties based on project requirements, primarily within Pharmaceutical, Biotechnology, or Biologics Regulatory Affairs, with potential involvement in related areas.
Contributing to regulatory submissions team activities, including preparation, compilation, and submission of regulatory documents such as CT/IND, MAA/NA, variations/lifecycle submissions, DSUR, PSUR, renewals, and agency briefing documentation.
Managing and implementing label review, translation requirements, fee calculations, and other aspects for regulatory submissions.
Providing input to the Regulatory Intelligence function and participating in readability testing.
Reviewing IMPD/IB Core Docs and labeling for clinical trials.
Collaborating with Regulatory Submissions team or cross-functional teams based on project size and nature.
Facilitating business development activities as needed.

Your Profile:

You will bring relevant regulatory affairs experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a relevant scientific discipline or healthcare-related field.
Familiarity with label review, translation requirements, and regulatory intelligence activities.
Strong attention to detail and excellent communication skills.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

Are you a current ICON Employee?

Apply Now

Refine Your Search

regulatory affairs specialist jobs in staines upon thames, sry

Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

Senior Regulatory Affairs Specialist

Sr. Specialist, Regulatory Affairs

Nutrition Specialist (Global Regulatory & Corporate Affairs)

Medical Information Specialist - US Hours

Senior Regulatory Specialist

Expert Consultant – Healthcare | Safety, Risk & Regulatory

Senior Manager – ESG and Sustainability Regulatory Legal

Director - Regulatory Affairs Lifecycle Management Non-Medicines

Medical Information Specialist - Afterhours

Account Executive - Agricultural Regulatory Intelligence

Regulatory Engagement & Advocacy Manager – UK and France

Medical Information Specialist - German & English speaking

Analyst - Regulatory Market Access and Compliance

Analyst

South & EE Team Regulatory Affairs Lead

Specialist, Quality Audits - Biosimilars

Director - Regulatory Affairs Lifecycle Management Medicines

UK & Europe Corporate Communications Lead

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