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

Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
CRA2 - Multi-Sponsor Department
IQVIA —Reading
- Full-time
- Remote
- No degree
- Work from home
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- Full-time
- No degree
- Travel
7d
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
11d
Associate Director Quality - Client Dedicated ( Regional Clinical Compliance Lead)
IQVIA —Reading
- Full-time
- Remote
- Management
- English
- Microsoft Office
- Work from home
6d
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Reading
- Full-time
- Hybrid work
- Management
- Doctoral degree
- Data analysis 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
Clinical Trial Supplies Associate ** Farnborough, UK **
Syneos - Clinical and Corporate - Prod —Farnborough
- Full-time
- English
- Microsoft Office
- Travel
Experienced CRA - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- No degree
Sr. CRA 1 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Trial Supplies Associate ** Farnborough, UK **
サイネオス・ヘルス —Farnborough
- English
- Microsoft Office
- Travel
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Project management
- Work from home
13d
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
CRA II, client-dedicated (fixed-term)
Fortrea —Maidenhead
- Full-time
- Travel
- Organisational skills
- Communication skills
Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International plc —Marlow
- £80,000 - £140,000 a year
- Full-time
- Bachelor's degree
- No degree
- Leadership
14d
Territory Manager, Vascular Access - North West
BD —Winnersh
- £43,300 - £66,025 a year
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Associate Director Global CMC QU – Clinical GMP/GDP
Kyowa Kirin International —Marlow
- £66,814 - £134,641 a year
- Full-time
- Bachelor's degree
- No degree
- Leadership
Quick apply
14d

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Clinical Trial Associate

ICON Plc -
Reading

Apply Now

Job details

Full-time

Benefits

Company pension
Employee assistance programme

Qualifications

Bachelor's degree
Organisational skills

Full job description

CTA

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.

Job title - CTA (relevant experience required)

Location - Must be within a commutable distance to London (2 days office presence required)

Fully sponsor dedicated

As a Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks.

What You Will Do:

You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges.

Key responsibilities include:

Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.
Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study.
Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials.
Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success.

Your Profile:

You will have a strong foundation in clinical trial management, with the experience to work independently and guide others.

Required qualifications and experience:

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.
Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively.
Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management.
Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders.
Willingness to travel as required (approximately 10%)

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 associate jobs in mortimer common, ham

Clinical Trial Associate

Clinical Research Associate II

CRA2 - Multi-Sponsor Department

Clinical Research Associate - IQVIA Biotech

CRA 2 - Single Sponsor Dedicated

Study Start Up Associate

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

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

Clinical Trial Supplies Associate Farnborough, UK

Experienced CRA - Single Sponsor Dedicated

Sr. CRA 1 - Single Sponsor Dedicated

Clinical Trial Supplies Associate Farnborough, UK

Local Study Associate Director

CRA

CRA II, client-dedicated (fixed-term)

Associate Director Global CMC QU – Clinical GMP/GDP

Territory Manager, Vascular Access - North West

Senior Clinical Research Associate

Associate Director Global CMC QU – Clinical GMP/GDP

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