Clinical associate Work, Jobs in Reading, Brk (with Salaries)

Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- Full-time
- No degree
- Travel
- Recruiting
14d
CRA
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme
4d
Clinical Research Associate I
Fortrea —Maidenhead
- Full-time
Associate Scientist, Translational Medicine
Immunocore —Oxford
- Master's degree
- Bachelor's degree
- Organisational skills
8d
Occupational Health Advisor/Vaccinator
Innovate HMG Ltd —Middlesex
- £38,000 - £45,000 a year
- Part-time
- In-person
- Health & wellbeing programme
- Work from home
Quick apply
6d
Warehouse Associate
Montu UK —Wokingham
- £30,000 - £32,000 a year
- Full-time
- Assembly
- Warehouse experience
- Manufacturing
- Free parking
Quick apply
5d
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Reading
- Full-time
- Hybrid work
- Doctoral degree
- English
- Master's degree
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Reading
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Business development
Compliance Administrator
Active Care Group —Thame
- £28 - £30 an hour
- Full-time
- Microsoft Outlook
- Administrative experience
- Organisational skills
Quick apply
Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry
Moderna, Inc. —Oxford
- Weekend availability
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Associate Publisher
Wiley —Oxford
- £31,400 - £43,800 a year
- Full-time
- Organisational skills
- Communication skills
1d
Senior Research Associate, Bioanalytical & Molecular Assays
Moderna, Inc. —Oxford
- Full-time
- Data analysis skills
- Bachelor's degree
- Annual leave
Associate Director, Clinical Trial Disclosure & Transparency
CSL Behring —Maidenhead
- Full-time
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Communication skills
1d
Quality Associate II, Quality Assurance
Replimune —Abingdon
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
Quick apply
General Practice Assistant
The Cambridge Practice —Aldershot
- £13 - £14 an hour
- Full-time
- Care plans
- Nursing
- Health & wellbeing programme
- Employee discount
Quick apply
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home
Senior Medical Information Associate Italian Language
PrimeVigilance —Guildford
- Full-time
- Remote
- Customer service
- English
- Communication skills
Quick apply
Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based
Moderna, Inc. —Oxford
- Weekend availability
- Microsoft Powerpoint
- Doctoral degree
- Data analysis skills
- Annual leave

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clinical associate jobs near reading, brk

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 associate jobs in reading, brk

Clinical Trial Associate

Clinical Research Associate - IQVIA Biotech

CRA

Clinical Research Associate I

Associate Scientist, Translational Medicine

Occupational Health Advisor/Vaccinator

Warehouse Associate

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Senior CRA

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Compliance Administrator

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

Associate Publisher

Senior Research Associate, Bioanalytical & Molecular Assays

Associate Director, Clinical Trial Disclosure & Transparency

Quality Associate II, Quality Assurance

General Practice Assistant

Local Study Associate Director

Senior Medical Information Associate Italian Language

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

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