Policy manager Work, Jobs in Newbury (with Salaries)

Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead
IQVIA —Reading
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's degree
- Work from home
9d
Senior Research Fellow and Programme Manager in Taiwan Studies
University of Oxford —Oxford
- £49,119 - £53,483 a year
- Full-time
- Doctoral degree
- Annual leave
11d
VodafoneThree - Compliance Monitoring & Testing Manager
Vodafone —Newbury
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Office
- Employee discount
10d
Associate Director Quality - Client Dedicated ( Regional Clinical Compliance Lead)
IQVIA —Reading
- Full-time
- Remote
- Management
- English
- Microsoft Office
- Work from home
4d
VodafoneThree - Financial Services Compliance Advice Manager
VodafoneThree —Newbury
- Full-time
- Hybrid work
- Employee discount
Quick apply
9d
Facilities Management and Compliance Lead
SouthOxfordshireAndVale —Abingdon
- £52,892 - £58,923 a year
- Maintenance
- Project management
- Continuous improvement
- Flexible schedule
Quick apply
Warehouse Process and Compliance Manager
Gist Limited —Basingstoke
- £55,000 - £65,000 a year
- Full-time
- Hybrid work
- Project management
- Annual leave
- Employee assistance programme
Medical Writing Manager – Patient Centered Solutions, Strategic & Scientific Research
IQVIA —Reading
- Full-time
- Hybrid work
- Microsoft Office
- Bachelor's degree
- Medical terminology
Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead
IQVIA —Reading
- Full-time
- Remote
- English
- Microsoft Office
- Analysis skills
- Work from home
6d
Research Grants Manager
University of Oxford —Oxford
- £39,424 - £51,983 a year
- Full-time
- Oracle
- Microsoft Office
- Contracts
Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection
IQVIA —Reading
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's degree
- Work from home
4d
Director, Remote Research Clinicians
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Communication skills
- Work from home
11d
Senior Compliance Manager
Oxford University Press —Oxford
- Full-time
- Hybrid work
- Management
- Travel
- Communication skills
- Employee discount
6d
DLP Policy Lead
Primark —Reading
- Analysis skills
- Communication skills
Compliance & Quality Manager
IQVIA —Reading
- Full-time
- Hybrid work
Private Client Compliance - Trusts Manager
Cooper Parry —Reading
- Full-time
- Remote
- Tax experience
Principal Minerals and Waste Policy Planner - Technical Lead
OXFORDSHIRE COUNTY COUNCIL —Oxford
- £50,269 - £53,460 a year
- Part-time
- Negotiation
2d
Trade Compliance Manager
Tekever —Swindon
- Hybrid work
- ERP systems
- Analysis skills
- Organisational skills
Quick apply
11d
Director, Oxford Research Technology
Vertex Pharmaceuticals —Oxford
- Full-time
- Bachelor's degree
- No degree
- Leadership
4d

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Senior Research Fellow and Programme Manager in Taiwan Studies
University of Oxford —Oxford
The post holder will specialize in Taiwan Studies whilst also having expertise in a disciplinary or interdisciplinary field including but not limited to…
£49,119 - £53,483 a year
11d

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Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead

IQVIA -
Reading

Apply Now

Job details

Full-time
9 days ago

Benefits

UK visa sponsorship
Work from home

Qualifications

Clinical research
Business processes
English
Microsoft Office
Bachelor's degree
Computer skills
Leadership
Communication skills
Negotiation

Full job description

Reading, United Kingdom | Full time | Home-based | R1558528

Job Description Summary

Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead is responsible for proactively identifying signals, trends, and systemic issues across countries and EMEA region to drive continuous improvement in clinical trial execution and processes. This role plays a key part in translating operational insights into actionable improvements, partnering with Global Clinical Compliance, RBQM (Risk-Based Quality Management), and global process owners to enhance efficiency, compliance, and quality across the organization.

Essential Functions of the Job:

Signal Detection & Trend Analysis

Identify and analyze signals, trends, and systemic issues across EMEA using compliance-generated data,

audit findings, inspection outcomes, and operational insights.

Translate aggregated insights into meaningful risk patterns and improvement opportunities.
Provide regular reporting and recommendations to stakeholders to support informed decision-making.

Process Improvement & Risk Management

Propose and support process improvements based on identified trends and systemic issues.
Collaborate closely with RBQM teams to integrate findings into process risk assessment and risk mitigation strategies.
Ensure alignment of improvements with GCP requirements, company procedures, and quality standards
Identify areas of additional training and support for preparing and delivering such educational sessions within the EMEA region

Operational Excellence & Implementation

Support regional and country-level process improvement initiatives to enhance efficiency, compliance, and consistency.
Act as a liaison between regional/country teams and Global Clinical Compliance and global process owners.
Facilitate the regional implementation of improvements identified at global, local or regional levels, ensuring scalability and sustainability.
Promote best practice sharing across countries and regions.

takeholder Collaboration & Influence

Partner cross-functionally with Clinical Operations, Quality Assurance, RBQM, and Global Compliance teams.
Influence stakeholders at multiple levels to drive the adoption of process enhancements.
Support change management activities related to new or updated processes.

Qualifications
Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline* with 10+ years in clinical research, clinical operations, plus minimum 4 years *experience in a GCP compliance or GCP quality.

Experience with RBQM principles, risk identification, and data-driven decision-making.
Experience in process improvement, operational excellence, or quality initiatives.
Certification in quality management, clinical research, or process improvement methodologies (e.g., Lean Six Sigma) will be a plus
Experience supporting or implementing global process changes
Experience in oncology global trials is preferred.
Requires deep knowledge of one or more related job areas typically obtained through advanced education combined with experience.
Sound working knowledge of relevant terminology, International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), applicable regulatory requirements, quality management processes.
Excellent organizational, interpersonal and communication skills.
Excellent judgement and decision-making skills.
Demonstrated leadership and line management skills.
Excellent influencing and negotiation skills.
Strong computer skills including Microsoft Office applications.
Excellent problem-solving skills.
Demonstrated ability to work in a matrix environment.
Ability to lead and motivate a clinical team also required.
Ability to travel within the region/country.
Ability to establish and maintain effective working relationships with co-workers, managers and clients.
Fluent in English.

Please note: this role is not eligible for the UK VISA sponsorship.

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

policy manager jobs in newbury

Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead

Senior Research Fellow and Programme Manager in Taiwan Studies

VodafoneThree - Compliance Monitoring & Testing Manager

Associate Director Quality - Client Dedicated ( Regional Clinical Compliance Lead)

VodafoneThree - Financial Services Compliance Advice Manager

Facilities Management and Compliance Lead

Warehouse Process and Compliance Manager

Medical Writing Manager – Patient Centered Solutions, Strategic & Scientific Research

Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead

Research Grants Manager

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

Director, Remote Research Clinicians

Senior Compliance Manager

DLP Policy Lead

Compliance & Quality Manager

Private Client Compliance - Trusts Manager

Principal Minerals and Waste Policy Planner - Technical Lead

Trade Compliance Manager

Director, Oxford Research Technology

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