Clinical research associate Work, Jobs in Egham, Sry (with Salaries)

Clinical Research 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
Research Associate Immunology Research
UCB —Slough
- Master's degree
- Bachelor's degree
- Communication skills
11d
Research Associate in Salmonella clinical study
Imperial College London —South Kensington
- £43,863 - £57,472 a year
- Full-time
- Hybrid work
- Doctoral degree
- University
- Organisational skills
Research Associate
Lumanity —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
Study Research Assistant
University College London —London
- £39,148 - £41,833 a year
- Full-time
- Bachelor's degree
- No degree
- Organisational skills
- Annual leave
- Employee assistance programme
2d
Clinical Research Associate - 12 months' monitoring experience required
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Clinical Contracts Associate
ICON Plc —Reading
- Full-time
- Remote
- Master's degree
- Analysis skills
- Bachelor's degree
- Employee assistance programme
11d
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Research Facilitator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
14d
Research Associate
Imperial College London —Hammersmith
- £49,017 - £57,472 a year
- Full-time
- Doctoral degree
- University
RWE Associate Clinical Project Manager – Oncology (FSP)
IQVIA —Reading
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
1d
Clinical Trial Associate Manager
Galderma —London
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
Senior Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
11d
Patient Recruitment Associate II
ICON Plc —Reading
- Full-time
- Marketing
- Analysis skills
- Bachelor's degree
- Employee assistance programme
Manager - Patient Experience Data
IQVIA —Reading
- Full-time
- Remote
- Project management
- IT
- Time management
5d
Clinical Quality Assurance - Program Lead (Associate Director)
Novartis —London
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
Regulatory Science and Policy Associate - VIE Contract
Sanofi —Reading
- English
- Communication skills
1d
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Study Manager, Clinical Operations
Orchard Therapeutics —London
- Full-time
- Hybrid work
- Doctoral degree
- English
- Project management
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Clinical Research Associate

ICON Plc -
Reading

Apply Now

Job details

Full-time

Benefits

Company pension
Employee assistance programme

Qualifications

Driving Licence
Clinical research
Bachelor's degree
Organisational skills
Communication skills

Full job description

Clinical Research Associate - Single Sponsor - 3/4 SIV's per month

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.

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 2 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational and communication skills, with attention to detail.

Ability to work independently and collaboratively in a fast-paced environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

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 here.

Apply Now

Refine Your Search

clinical research associate jobs in egham, sry

Clinical Research Associate

Clinical Research Associate II

Research Associate Immunology Research

Research Associate in Salmonella clinical study

Research Associate

Study Research Assistant

Clinical Research Associate - 12 months' monitoring experience required

Clinical Contracts Associate

Senior Clinical Research Associate

Research Facilitator

Research Associate

RWE Associate Clinical Project Manager – Oncology (FSP)

Clinical Trial Associate Manager

Senior Clinical Trial Associate

Patient Recruitment Associate II

Manager - Patient Experience Data

Clinical Quality Assurance - Program Lead (Associate Director)

Regulatory Science and Policy Associate - VIE Contract

Specialist, R&D Contracts & Business Operations

Study Manager, Clinical Operations

I want to receive the latest job alerts for clinical research associate in egham, sry

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