Clinical trial manager Work, Jobs in Chilton, Oxf (with Salaries)

Clinical Trial Manager
ICON Plc —Reading
- Full-time
- Employee assistance programme
4d
Sr. CRA 1 - Site Management
IQVIA —Reading
- Full-time
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Work from home
Trial Manager
University of Oxford —Oxford
- £39,424 - £47,779 a year
- Part-time
- Project management
- Annual leave
7d
Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead
IQVIA —Reading
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's degree
- Work from home
11d
Senior Clinical Technology Specialist
IQVIA —Reading
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- SharePoint
- Work from home
Research Assistant
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Full-time
- Laboratory experience
- Bachelor's degree
- Organisational skills
Clinical Specialist, Cryo Nerve Block
AtriCure International —Swindon
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
- Annual leave
Clinical Trials Manager
University of Oxford —Oxford
- £34,982 - £44,382 a year
- Full-time
- No degree
- Organisational skills
- Communication skills
13d
Clinical FSP Director Quality - Client Dedicated- Regional Clinical Compliance Inspection Lead
IQVIA —Reading
- Full-time
- Remote
- English
- Microsoft Office
- Analysis skills
- Work from home
8d
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
Clinical Registry Coordinator
ICON Plc —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
- Employee assistance programme
5d
da Vinci Cardiovascular Program Specialist
Intuitive Surgical —Reading
- Day shift
- Nursing
- Anatomy knowledge
- Bachelor's degree
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Associate Director Quality - Client Dedicated ( Regional Clinical Compliance Lead)
IQVIA —Reading
- Full-time
- Remote
- Management
- English
- Microsoft Office
- Work from home
6d
Clinical Operations Manager
University of Oxford —Oxford
- £49,119 - £58,265 a year
- Full-time
- Organisational skills
- Communication skills
12d
Connected Devices - Primary analyst, Spirometry
IQVIA —Reading
- Full-time
- Remote
- Computer literacy
- Work from home
Clinical Research Administator
University of Oxford —Oxford
- £32,108 - £40,514 a year
- Full-time
- Oracle
- Administrative experience
- Organisational skills
Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection
IQVIA —Reading
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's degree
- Work from home
6d
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Medical Strategy Lead, Oncology (Home-Based)
IQVIA —Reading
- Full-time
- Remote
- Microsoft Outlook
- English
- Business development
- Work from home

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clinical trial manager jobs near chilton, oxf

Clinical Trial Manager

ICON Plc -
Reading

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Job details

Full-time
4 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Clinical research

Full job description

Clinical Trial Manager - Oncology

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.

Clinical Trial Manager - Oncology (Late Development)

Location: Home-based, UK

At ICON, our people drive innovation and help shape the future of clinical development. As a Clinical Trial Manager within our client's Late Development Oncology team, you will play a critical role in leading the operational delivery of global clinical studies, ensuring the successful execution of complex oncology programmes while maintaining the highest standards of quality, compliance, and patient safety.

This is an opportunity to join a high-performing team and contribute to cutting-edge oncology research that supports the development of life-changing therapies for patients worldwide.

What You Will Do

As a Clinical Trial Manager, you will provide operational leadership across all phases of study delivery, collaborating with internal and external stakeholders to ensure clinical trials are executed efficiently, on time, and in compliance with all applicable regulations and quality standards.

Key responsibilities include:

Lead the planning, execution, and oversight of clinical trial activities, ensuring delivery against timelines, budgets, and key study milestones.
Partner with cross-functional teams to develop and implement study-specific operational plans, processes, and procedures.
Build and maintain strong relationships with investigators, study sites, vendors, and key stakeholders to support successful study outcomes.
Monitor study progress, proactively identify risks, and implement mitigation strategies to ensure continued operational excellence.
Ensure studies are conducted in accordance with ICH-GCP guidelines, protocol requirements, and all applicable local and international regulatory standards.
Oversee vendor performance and contribute to vendor selection, management, and governance activities where appropriate.
Drive issue resolution and support critical decision-making related to study conduct, quality, and operational delivery.
Act as a key point of contact for internal and external stakeholders, providing regular updates on study progress, risks, and achievements.

About You

You are an experienced Clinical Trial Manager with a proven track record of successfully delivering oncology clinical studies in a commercial clinical research environment. You combine strong operational expertise with excellent stakeholder management skills and the ability to navigate competing priorities in a fast-paced setting.

To be successful in this role, you will bring:

A degree in Life Sciences, Medicine, Pharmacy, Nursing, or a related scientific discipline, or an equivalent combination of education and relevant experience.
Demonstrated experience leading the operational delivery of clinical trials and driving study outcomes against key performance indicators.
Strong understanding of clinical trial regulations, ICH-GCP requirements, and industry best practices.
Experience working within a commercial pharmaceutical, biotechnology, or CRO environment.
Prior clinical monitoring experience is advantageous.
Significant experience managing Oncology clinical trials, ideally within late-phase development programmes.
Excellent communication, organisational, and problem-solving skills, with the ability to influence and collaborate across diverse stakeholder groups.

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

clinical trial manager jobs in chilton, oxf

Clinical Trial Manager

Sr. CRA 1 - Site Management

Trial Manager

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

Senior Clinical Technology Specialist

Research Assistant

Clinical Specialist, Cryo Nerve Block

Clinical Trials Manager

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

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Clinical Registry Coordinator

da Vinci Cardiovascular Program Specialist

Senior Clinical Data Manager - sponsor dedicated - oncology

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

Clinical Operations Manager

Connected Devices - Primary analyst, Spirometry

Clinical Research Administator

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

CRA 2 - Single Sponsor Dedicated

Medical Strategy Lead, Oncology (Home-Based)

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