Clinical research associates & coordinators 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 Registry Coordinator - UK Based
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
5d
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
Clinical Registry Coordinator
ICON Plc —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
- Employee assistance programme
5d
CRA 2 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
12d
Experienced CRA - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- No degree
Senior Clinical Technology Specialist
IQVIA —Reading
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- SharePoint
- Work from home
Sr. CRA 1 - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)
IQVIA —Reading
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Data analysis skills
- Work from home
Site Enrollment and Engagement Lead
IQVIA —Reading
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
- Work from home
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Part-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
Quick apply
14d
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Clinical Trial Manager
ICON Plc —Reading
- Full-time
- Employee assistance programme
4d
CRA II, client-dedicated (fixed-term)
Fortrea —Maidenhead
- Full-time
- Travel
- Organisational skills
- Communication skills

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clinical research associates & coordinators jobs near mortimer common, ham

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 research associates & coordinators jobs in mortimer common, ham

Clinical Trial Associate

Clinical Registry Coordinator - UK Based

Clinical Research Associate II

CRA2 - Multi-Sponsor Department

Clinical Research Associate - IQVIA Biotech

Clinical Registry Coordinator

CRA 2 - Single Sponsor Dedicated

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Study Start Up Associate

Experienced CRA - Single Sponsor Dedicated

Senior Clinical Technology Specialist

Sr. CRA 1 - Single Sponsor Dedicated

Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)

Site Enrollment and Engagement Lead

CRA

Clinical Research Scientist

Senior Clinical Data Manager - sponsor dedicated - oncology

Senior Clinical Research Associate

Clinical Trial Manager

CRA II, client-dedicated (fixed-term)

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