Regulatory affairs lead Work, Jobs in Datchet, Brk (with Salaries)

Patient-Centered Outcomes Research (PCOR) Lead (UK)
UCB —Slough
- Doctoral degree
- Master's degree
- Leadership
Medical Affairs Coordinator
Servier —Slough
- Microsoft Office
- Databases
- Administrative experience
Quality Assurance & Regulatory Affairs Executive - Maternity Cover
TensCare Ltd —Epsom
- £35,000 - £42,500 a year
- Temporary
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Team management
- Profit sharing
- Work from home
Quick apply
Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK
Cepheid —Amersham
- Full-time
- Remote
- Master's degree
- Databases
- Bachelor's degree
- Annual leave
Regulatory, Data Protection and Ethics Lead
Foundation Partners —London
- Hybrid work
- AI
- Negotiation
Quick apply
Senior ESG Regulatory Operations Associate
Ralph Lauren —London
- Full-time
- Continuous improvement
- Organisational skills
EU Regulatory Affairs Manager
Amgen —London
- £48,957 - £66,237 a year
- Remote
- Research
- Conflict management
- AI
- Work from home
Global Value, Access & Government Affairs Lead
Mundipharma —London
- Full-time
- Doctoral degree
- Research
- Master's degree
PV Systems and Processes Lead x2
CSL Seqirus —Maidenhead
- Full-time
- Continuous improvement
- No degree
- Leadership
Sr Director, Drug Development Lead
IQVIA —Reading
- Full-time
- Remote
- Management
- Doctoral degree
- Master's degree
- Work from home
7d
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home
Professional Veterinary Affairs Manager UK & Ireland (175066)
Colgate-Palmolive —Surrey
- £70,650 - £78,500 a year
- Doctoral degree
- Sales
- Business development
Medical Advisor
Norgine —Uxbridge
- Full-time
- Hybrid work
Quick apply
Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Nursing
- Doctoral degree
- Master's degree
Quick apply
Regulatory Compliance Supervisor (m/f/x)
3M —Bracknell
- Full-time
- Engineering
- Research
- Master's degree
- Flexible schedule
GB Sr. Manager, Regulatory Affairs - Europe
The Bountiful Company —London
- Writing skills
- Bachelor's degree
- Training & development
Quick apply
Senior Benefits Risk Management Lead
Bayer —Reading
- £110,000 - £130,000 a year
- Full-time
- Hybrid work
- English
- Databases
- Continuous improvement
- Annual leave
- Employee discount
Global Manager, Performance Validation - Personal Care
Elementis —Ascot
- Full-time
- Hybrid work
- English
- Bachelor's degree
- Quality control
Global Medical Affairs Associate Director - Metabolic & Dermato-Oncology
Recordati —Hemel Hempstead
- Full-time
- Hybrid work
- English
- Quality control
- Travel
Expert Consultant – Healthcare | Safety, Risk & Regulatory
Boston Consulting Group —London
- Full-time
- Doctoral degree
- Master's degree
- Business development

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regulatory affairs lead jobs near datchet, brk

Patient-Centered Outcomes Research (PCOR) Lead (UK)

UCB -
Slough

Apply Now

Job details

Permanent

Qualifications

Clinical research
Doctoral degree
Stakeholder collaboration
Stakeholder liaison
Master's degree
Partnership building
Multidisciplinary collaboration
Project leadership
Leadership
Project management experience

Full job description

Make your mark for patients

We are looking for a Patient-Centered Outcomes Research (PCOR) Lead who is strategic, collaborative, and insightful to join our Patient-Centered Outcomes Research (PCOR) team, based at our UCB headquarter located in Brussels, Belgium, or in our offices in Monheim Germany, or Slough UK.

About the role

As a PCOR Lead, you will play a leading role in the development and implementation of patient-reported outcomes (PRO) and more broadly clinical outcome assessment (COA) strategies. You will generate robust patient experience data and evidence that demonstrate the meaningful patient benefits of our innovative UCB solutions and that meet external evidentiary standards and support healthcare decision-making.

Who you will work with

As a member of the Patient-Centered Outcomes Research team, you will collaborate with cross-functional teams, eg, representatives from Clinical Development, Medical Affairs, Health Economics and Outcomes Research, Market Access, Regulatory Affairs, and Biostatistics.

What you will do

You will lead the development and implementation of patient experience evidence strategy on clinical outcome assessments (COAs) from early development through to full lifecycle management.
You will lead research activities supporting the selection, development, validation, interpretation, and implementation of PRO/COA measures.
You will provide subject matter expert input into strategic documents, tactical plans and target patient value profiles, as well as into clinical documents, eg, study protocols, analysis plans, clinical reports.
You will provide subject matter expert input into regulatory and HTA briefing packages and interactions..
You will lead scientific dissemination (eg, peer-reviewed publications, abstracts) in line with publication strategies.
You will build relationships and partner with external groups to advance methodological frameworks and acceptance of patient experience evidence to inform external healthcare decision making.
You will be an inspiring ambassador to contribute to organizational awareness on the value of patient experience evidence.

Interested? For this role, we are looking for the following education, experience, and skills:

Master's degree, PhD, MD, or equivalent qualification in a relevant scientific discipline.
Significant experience in biopharmaceutical, medical device, or academic environments within PRO/COA, or patient preference research.
Expertise in PRO/COA development, validation, and implementation in clinical research, including strong knowledge of qualitative and quantitative scientific methodologies and evidentiary requirements by regulatory and HTA bodies
Experience in clinical development, regulatory and HTA interactions.
Excellent stakeholder management, communication, influencing, and cross-functional collaboration skills in a matrix organization.
Proven project leadership capabilities with experience managing complex global initiatives

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [email protected]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Apply Now

Refine Your Search

regulatory affairs lead jobs in datchet, brk

Patient-Centered Outcomes Research (PCOR) Lead (UK)

Medical Affairs Coordinator

Quality Assurance & Regulatory Affairs Executive - Maternity Cover

Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

Regulatory, Data Protection and Ethics Lead

Senior ESG Regulatory Operations Associate

EU Regulatory Affairs Manager

Global Value, Access & Government Affairs Lead

PV Systems and Processes Lead x2

Sr Director, Drug Development Lead

Local Study Associate Director

Professional Veterinary Affairs Manager UK & Ireland (175066)

Medical Advisor

Drug Safety Associate II

Regulatory Compliance Supervisor (m/f/x)

GB Sr. Manager, Regulatory Affairs - Europe

Senior Benefits Risk Management Lead

Global Manager, Performance Validation - Personal Care

Global Medical Affairs Associate Director - Metabolic & Dermato-Oncology

Expert Consultant – Healthcare | Safety, Risk & Regulatory

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