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

Clinical Research Associate - 12 months' monitoring experience required
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
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
Clinical Research Assistant / Clinical Research Practitioner
Oxford Health NHS Foundation Trust —Oxford
- £32,073 - £39,043 a year
- Full-time
- Annual leave
- Employee assistance programme
8d
Research Assistant (Nutrition)
Oxford Brookes University —Headington
- £32,080 - £34,610 a year
- Full-time
- Hybrid work
- University
10d
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Research Assistant
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Full-time
- Laboratory experience
- Bachelor's degree
5d
Research Assistant: Cognitive Neuroscience
University of Oxford —Oxford
- £35,681 - £38,366 a year
- Psychology
- Annual leave
5d
Research Facilitator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
Clinical Contracts Associate
ICON Plc —Reading
- Full-time
- Remote
- Master's degree
- Analysis skills
- Bachelor's degree
- Employee assistance programme
11d
Project Manager, Remote Research Clinicians
IQVIA —Reading
- Full-time
- English
- Project management
- Bachelor's degree
Research Associate Immunology Research
UCB —Slough
- Master's degree
- Bachelor's degree
- Communication skills
12d
Research Assistant - All About Me project OCEMR
University of Oxford —Oxford
- £35,681 - £37,338 a year
- Hybrid work
- Bachelor's degree
- Psychology
- In-person
- Annual leave
9d
Clinical Project Manager I
Perspectum —Oxford
- £33,000 - £45,000 a year
- Full-time
- Project management
- Communication skills
Quick apply
Regulatory and Start Up Specialist - UK
IQVIA —Reading
- Full-time
- Remote
- Maintenance
- Bachelor's degree
- Referral programme
3d
RWE Clinical Project Manager – Oncology (FSP)
IQVIA —Reading
- Full-time
- Remote
- Project management
- Bachelor's degree
- Continuous improvement
2d
Global Study Lead
ICON Plc —Reading
- Full-time
- Management
- PMP
- Project management
- Employee assistance programme
12d
Research Assistant: Psychopharmacology and Emotion Research
University of Oxford —Oxford
- £35,681 - £37,338 a year
- Full-time
- Master's degree
- Annual leave
3d
Practice Liaison Officer / Research Facilitator
University of Oxford —Oxford
- £35,681 - £41,636 a year
- Full-time
- Remote
3d
(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry
Moderna, Inc. —Oxford
- Full-time
- Laboratory experience
- Microsoft Office
- Presentation skills
- Annual leave

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clinical research jobs near reading, brk

Clinical Research Associate - 12 months' monitoring experience required

ICON Plc -
Reading

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Job details

Full-time

Benefits

Company pension
Employee assistance programme

Qualifications

Clinical research
Bachelor's degree
Organisational skills
Communication skills

Full job description

CRA

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 - CRA (must have at least 12 months' monitoring experience)

Location - Must be based in the UK

Fully sponsor dedicated

Working fully embedded within a growing program as a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

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:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 12 months experience as a Clinical Research Associate.
Must have experience working on Oncology trials
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.
Willingness to travel as required (approximately 60%)

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 jobs in reading, brk

Clinical Research Associate - 12 months' monitoring experience required

Clinical Research Associate

Clinical Research Associate II

Clinical Research Assistant / Clinical Research Practitioner

Research Assistant (Nutrition)

Senior Clinical Research Associate

Research Assistant

Research Assistant: Cognitive Neuroscience

Research Facilitator

Clinical Contracts Associate

Project Manager, Remote Research Clinicians

Research Associate Immunology Research

Research Assistant - All About Me project OCEMR

Clinical Project Manager I

Regulatory and Start Up Specialist - UK

RWE Clinical Project Manager – Oncology (FSP)

Global Study Lead

Research Assistant: Psychopharmacology and Emotion Research

Practice Liaison Officer / Research Facilitator

(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

I want to receive the latest job alerts for clinical research in reading, brk

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