Regulatory affairs manager Work, Jobs in Hare Hatch, Brk (with Salaries)

Study Start Up Manager
Fortrea —Maidenhead
- Full-time
- Remote
- English
- Bachelor's degree
9h
Regulatory Affairs Manager
pladis —Chiswick Park Station
- Full-time
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Product Manager, Surgical Solutions - UK
BD —Winnersh
- £43,300 - £66,025 a year
- English
- Bachelor's degree
- Product management
1d
Commercial Manager
Archit Pharma Innovations Ltd —Cox Green
- £34,000 - £36,000 a year
- Full-time
- CRM software
- Microsoft Office
- Business development
Quick apply
Global Manager, Performance Validation - Personal Care
Elementis —Ascot
- Full-time
- Hybrid work
- English
- Bachelor's degree
- Quality control
2d
Democratic Services Officer
Royal Borough of Windsor and Maidenhead —Maidenhead
- £30,193 - £34,104 a year
- Full-time
- Hybrid work
- English
- Organisational skills
- Communication skills
- Free parking
- Annual leave
5d
Medical Affairs Coordinator
Servier —Slough
- Microsoft Office
- Databases
- Administrative experience
9d
Regulatory Quality Assurance Manager
Alliance Medical Ltd —Guildford
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Continuous improvement
Quick apply
Vice President, Regulatory Affairs – ELMAC
Amgen —Uxbridge
- Doctoral degree
- Master's degree
- Bachelor's degree
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home
Application Manager
Veterinary Medicines Directorate —New Haw
- £38,795 a year
- Part-time
- Microsoft Outlook
- Customer service
- Data analysis skills
- Free parking
- Annual leave
2d
Scientist, Performance Validation - Personal Care
Elementis —Ascot
- Full-time
- English
- Bachelor's degree
- Continuous improvement
4d
Solutions Consultant- UK/Europe
MasterControl —Basingstoke
- Presentation skills
- Bachelor's degree
- No degree
- Annual leave
- Life insurance
Operations Manager
Veterinary Medicines Directorate —New Haw
- £38,795 a year
- Part-time
- Microsoft Outlook
- Databases
- Analysis skills
- Free parking
- Annual leave
Brand Manager
Orion Corporation —Reading
- Full-time
- Hybrid work
- Marketing
- Analysis skills
- Project management
8d
Senior Technical Policy Executive
The Horticultural Trades Association —Didcot
- £35,000 - £40,000 a year
- Full-time
- Hybrid work
- CRM software
- Analysis skills
- Presentation skills
- Free parking
- Health & wellbeing programme
Quick apply
7d
PV Officer, Team Lead (Japanese Fluency required )
PrimeVigilance —Guildford
- Full-time
- Remote
- Nursing
- English
- Team management
Quick apply
Executive Director, Haematology/Oncology Business Unit Lead, UK & Ireland
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Sales
- English
- Master's degree
5d
Product Marketing Manager (Trust)
Revolut —London
- Marketing
13d

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regulatory affairs manager jobs near hare hatch, brk

Study Start Up Manager

Fortrea -
Maidenhead

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Job details

Full-time
9 hours ago

Qualifications

Healthcare research operations
Clinical research
Stakeholder collaboration
Stakeholder liaison
Process improvement
English
Bachelor's degree
Project schedule tracking
Multidisciplinary collaboration
Good Clinical Practice (GCP)
Good Clinical Practice (ICH-GCP) guidelines
Project progress tracking

Full job description

Join our Clinical Operations Team in a client-dedicated (FSP) role , supporting a leading global pharmaceutical company. This is a home-based position in the UK , where you will play a key role in driving global study start-up activities, site activation strategies, and operational excellence across international clinical trials.

This is an excellent opportunity for an experienced clinical research professional with a background in Study Start-Up, site activation, and regulatory submissions who enjoys working in a collaborative, fast-paced global environment.

What You'll Do

Support and oversee Study Start-Up activities from site identification through site activation.
Drive site activation timelines and proactively manage risks, escalations, and study milestones.
Contribute to the development and execution of global Study Start-Up strategies.
Coordinate regulatory submissions, Ethics Committee/IRB approvals, and site activation documentation.
Collaborate with study teams, regulatory functions, external vendors, and other stakeholders to support successful trial delivery.
Provide project updates and ensure timely completion of key deliverables.
Support implementation of clinical systems, reporting tools, and process improvement initiatives.
Contribute to the preparation and review of essential study documentation, ICFs, and regulatory submission packages.

What We're Looking For

Bachelor's degree in Life Sciences or a related field.
5+ years of experience in clinical research, Study Start-Up, site activation, regulatory affairs, or a related area.
Strong understanding of clinical trial conduct, including global and multi-center studies.
Experience with site activation activities and regulatory submissions.
Solid knowledge of ICH-GCP guidelines and regulatory requirements.
Proven project management and stakeholder management skills.
Excellent communication, organizational, and problem-solving abilities.

Preferred Experience

Working across multiple countries and regions within a global clinical trial environment.
Partnering with cross-functional teams and external service providers.
Supporting process improvement and operational excellence initiatives.

Why Join Us?

Dedicated partnership with a leading global pharmaceutical sponsor.
Opportunity to influence global study start-up strategies and processes.
Exposure to international, multi-center clinical trials.
Collaborative and supportive team environment.
Career growth opportunities within a global clinical research organization.

Learn more about our EEO & Accommodations request here .

Apply Now

Refine Your Search

regulatory affairs manager jobs in hare hatch, brk

Study Start Up Manager

Regulatory Affairs Manager

Senior Regulatory Affairs Specialist

Product Manager, Surgical Solutions - UK

Commercial Manager

Global Manager, Performance Validation - Personal Care

Democratic Services Officer

Medical Affairs Coordinator

Regulatory Quality Assurance Manager

Vice President, Regulatory Affairs – ELMAC

Local Study Associate Director

Application Manager

Scientist, Performance Validation - Personal Care

Solutions Consultant- UK/Europe

Operations Manager

Brand Manager

Senior Technical Policy Executive

PV Officer, Team Lead (Japanese Fluency required )

Executive Director, Haematology/Oncology Business Unit Lead, UK & Ireland

Product Marketing Manager (Trust)

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