Clinical trial manager Work, Jobs in Mortimer Common, Ham (with Salaries)

Clinical Trial Manager - Project Lead
ICON Plc —Reading
- Full-time
- Oracle
- Management
- Project management
- Employee assistance programme
2d
Sr. CRA 1 - Site Management
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Clinical Data Management Lead, home-based
IQVIA —Reading
- Remote
- Anatomy knowledge
- Customer service
- Project management
Territory Manager, Vascular Access - North West
BD —Winnersh
- £43,300 - £66,025 a year
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Specialist, Cryo Nerve Block
AtriCure International —Reading
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
- Annual leave
da Vinci Cardiovascular Program Specialist
Intuitive Surgical —Reading
- Day shift
- Nursing
- Anatomy knowledge
- Bachelor's degree
Senior Clinical Technology Specialist
IQVIA —Reading
- Analysis skills
- Bachelor's degree
- SharePoint
Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead
IQVIA —Reading
- English
- Microsoft Office
- Bachelor's degree
2d
Senior Medical Writer
IQVIA —Reading
- Doctoral degree
- Computer literacy
- Master's degree
13d
Project Manager I, IDEA
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Communication skills
- Employee assistance programme
4d
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Global Clinical Project Manager - Sponsor Dedicated
IQVIA —Reading
- Full-time
- Project management
- Bachelor's degree
- No degree
12d
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Solutions Consultant- UK/Europe
MasterControl —Basingstoke
- Microsoft Office
- Presentation skills
- Bachelor's degree
- Annual leave
- Life insurance
3d
Local Study Associate Director
IQVIA —Reading
- Patient monitoring
- English
- Project management
4d
Sr. CRA 1 - Single Sponsor Dedicated
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Territory Manager, Vascular Access Management (VAM) - South West
BD —Winnersh
- £43,300 - £66,025 a year
- Sales
- Organisational skills
- IT
Vendor Startup Manager IRT – Single Sponsor (home-based)
IQVIA —Reading
- Remote
- Continuous improvement
- Communication skills

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Clinical Trial Manager - Project Lead

ICON Plc -
Reading

Apply Now

Job details

Full-time
2 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Oracle
Management
Clinical research
Project management
Bachelor's degree
Leadership
FDA regulations

Full job description

Clinical Trial Manager - Project Lead

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.

As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.

What You Will Do:

You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.

Key responsibilities include:

Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
Train and mentor new CTA and LCRA staff.
Train the CTA and LCRA team in new processes or process updates.
Assign work across the team.
Monitor the progress of deliverables.
Run, review, and analyze reports for accuracy and work with the project teams to ensure updates are completed correctly.
Prepare reports on the status of deliverables and Hub progress to be presented to the project teams.

Your Profile:

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

University degree in medicine, science, or equivalent combination of education & experience
5+ years in clinical research, with substantial experience in clinical trial management, project management, or related roles.
Leadership Experience: Proven experience in leading study teams, managing cross-functional teams, or supervising junior CTMs and CRAs is essential.
Knowledge of Regulatory Requirements: Strong understanding of GCP, ICH guidelines, FDA regulations, and other relevant global regulatory requirements.
Clinical Trial Systems: Proficiency in CTMS, EDC, eTMF, and systems like Veeva Vault, Oracle, and Medidata is highly valued for managing data, timelines, and trial documentation.
Budget and Resource Management: Experience in managing study budgets, forecasting resources, and coordinating with finance or procurement for trial supplies.
Project Planning and Oversight: Ability to develop and manage project plans, timelines, and milestone tracking to ensure studies stay on schedule and within budget.
Vendor and Site Oversight: Experience in managing third-party vendors, such as CROs, labs, and other service providers, as well as maintaining strong relationships with trial sites.

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 mortimer common, ham

Clinical Trial Manager - Project Lead

Sr. CRA 1 - Site Management

Sr. Clinical Project Manager (Europe)

Clinical Data Management Lead, home-based

Territory Manager, Vascular Access - North West

Clinical Specialist, Cryo Nerve Block

da Vinci Cardiovascular Program Specialist

Senior Clinical Technology Specialist

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

Senior Medical Writer

Project Manager I, IDEA

Senior Clinical Data Manager - sponsor dedicated - oncology

Global Clinical Project Manager - Sponsor Dedicated

Senior Clinical Programmer I

Solutions Consultant- UK/Europe

Local Study Associate Director

Sr. CRA 1 - Single Sponsor Dedicated

CRA 2 - Single Sponsor Dedicated

Territory Manager, Vascular Access Management (VAM) - South West

Vendor Startup Manager IRT – Single Sponsor (home-based)

I want to receive the latest job alerts for clinical trial manager in mortimer common, ham

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