Associate director regulatory affair Work, Jobs in London (with Salaries)

Associate Director, Regulatory Innovation
IQVIA —London
- Full-time
- Remote
- Bachelor's degree
- No degree
- AI
- Work from home
12d
CMC Associate Director
Androlabs —London
- £85,000 - £108,000 a year
- Full-time
- Hybrid work
- Management
- Project management
- IT
- Annual leave
Quick apply
13d
Associate Director (Public Affairs - Tech Policy & Regulation)
Hanbury Strategy —London
- Hybrid work
- Presentation skills
- Communication skills
- Health & wellbeing programme
- Annual leave
Associate Director, CMC Regulatory Affairs (Hematology/Oncology)
Regeneron —Uxbridge
- Bachelor's degree
- IT
- In-person
- Annual leave
Associate Director - Regulatory Affairs Operations
Perrigo —London
- Hybrid work
- In-person
- Leadership
Associate Director, Regulatory Diagnostics
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Communication skills
- Negotiation
Associate Director, Resilience Strategic Partnerships – UK
Moderna, Inc. —London
- Full-time
- Master's degree
- Project management
- Agile
- Annual leave
Associate Director (Public Affairs)
Hanbury Strategy —London
- Hybrid work
- Presentation skills
- Communication skills
- Health & wellbeing programme
- Annual leave
5d
Senior Manager/Associate Director, Government and Regulatory Affairs
Access Partnership —London
- Hybrid work
Quick apply
Vice President / Associate Director, Crisis & Risk
Edelman —London
- Full-time
- Project management
- IT
Associate Director, Global Regulatory Science, CMC
Moderna, Inc. —London
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
- Annual leave
Associate Director, CMC Regulatory Affairs, International
Moderna, Inc. —London
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
- Annual leave
Senior Manager/Associate Director
Access Partnership —London
- Remote
Clinical Research Associate - Midlands
MSD —London
- Full-time
- English
- Microsoft Office
- Bachelor's degree
Associate Director, Global Medical Affairs (2-year contract)
BioNTech AG —London
- Full-time
- Doctoral degree
- Project management
- Travel
12d
Vice President / Associate Director, Crisis & Risk
Daniel J. Edelman Holdings —London
- Full-time
- Project management
- IT
Associate Director, IMACE Scientific Content, NS
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Doctoral degree
- English
- Organisational skills
6d
Global Medical Affairs Associate Director - Metabolic & Dermato-Oncology
Recordati —Hemel Hempstead
- Full-time
- Hybrid work
- English
- Travel
- In-person
2d
(Senior) Director Global Medical Affairs
BioNTech AG —London
- £168,100 - £318,300 a year
- Full-time
- Doctoral degree
- Travel
- Leadership
Associate Director (Internal Comms) - Burson
Burson Global —London
- Hybrid work
- AI

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Associate Director, Regulatory Innovation

IQVIA -
London

Apply Now

Job details

Full-time
12 days ago

Benefits

Work from home

Qualifications

Programme management
Business processes
Change management
Bachelor's degree
AI
Leadership

Full job description

London, United Kingdom | Full time | Home-based | R1556343

Job Description Summary

The Associate Director, Regulatory Innovation & Technology is responsible for driving innovation, process transformation, and technology enablement across Global Regulatory Affairs. This role partners with business leaders, technology teams, and strategic stakeholders to identify opportunities for operational improvement, define technology roadmaps, and lead the implementation of innovative solutions that enhance service delivery, quality, and efficiency.

A key responsibility is leading Regulatory Innovation Council activities, facilitating the evaluation, prioritization, and execution of innovation initiatives aligned with business strategy. The role serves as a bridge between business needs and technology capabilities, ensuring successful adoption of new processes, digital solutions, automation, and AI-enabled technologies.

Key Responsibilities

Lead Regulatory Innovation Council activities, including intake, evaluation, prioritization, and governance of innovation initiatives.
Drive business transformation through Lean process improvement, change management, and technology adoption activities.
Develop and manage innovation and technology roadmaps aligned with organizational objectives.
Partner with business stakeholders, technology teams, and strategic partners to define solution requirements and delivery plans.
Oversee complex innovation and technology programs, including scope, timelines, risks, dependencies, success metrics, and stakeholder communications.
Identify opportunities for automation, analytics, AI, and digital solutions that improve operational efficiency and service delivery.
Support technology design, development, pilot programs, and implementation of next-generation regulatory solutions.
Monitor industry, regulatory, and technology trends and translate insights into actionable business opportunities.
Build stakeholder engagement, secure sponsorship, and drive organizational readiness for change.
Mentor team members and foster a culture of innovation and continuous improvement.

Qualifications

Bachelor's degree or equivalent experience.
10+ years of experience in regulatory affairs, business transformation, technology enablement, product management, program management, or related fields.
Experience leading cross-functional initiatives involving process improvement, technology implementation, or organizational change.
Strong understanding of Lean methodologies, change management principles, and project/program governance.
Familiarity with AI, automation, analytics, and digital technologies within a professional services or life sciences environment.
Excellent communication, stakeholder management, facilitation, and leadership skills.
Demonstrated ability to influence across functions and drive adoption of new processes and technologies.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

associate director regulatory affair jobs in london

Associate Director, Regulatory Innovation

CMC Associate Director

Associate Director (Public Affairs - Tech Policy & Regulation)

Associate Director, CMC Regulatory Affairs (Hematology/Oncology)

Associate Director - Regulatory Affairs Operations

Associate Director, Regulatory Diagnostics

Associate Director, Resilience Strategic Partnerships – UK

Associate Director (Public Affairs)

Senior Manager/Associate Director, Government and Regulatory Affairs

Vice President / Associate Director, Crisis & Risk

Associate Director, Global Regulatory Science, CMC

Associate Director, CMC Regulatory Affairs, International

Senior Manager/Associate Director

Clinical Research Associate - Midlands

Associate Director, Global Medical Affairs (2-year contract)

Vice President / Associate Director, Crisis & Risk

Associate Director, IMACE Scientific Content, NS

Global Medical Affairs Associate Director - Metabolic & Dermato-Oncology

(Senior) Director Global Medical Affairs

Associate Director (Internal Comms) - Burson

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