Clinical research associate Work, Jobs in Iver, Bkm (with Salaries)

Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Specialist, R&D Contracts & Business Operations
CSL Behring —Maidenhead
- Full-time
- Bachelor's degree
- Organisational skills
- Contracts
Associate Dean (Research and Innovation) - Faculty of Health and Medical Sciences
University of Surrey —Guildford
- Full-time
- University
Research Fellow in Brain Vascular Biology and Brain Cancer Biology
University College London —London
- £43,374 - £51,860 a year
- Full-time
- Doctoral degree
- English
- University
- Annual leave
- Employee assistance programme
Associate Director, Clinical Trial Lead (all genders)
Merck KGaA —London
- Doctoral degree
- Master's degree
- Project management
4d
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Project management
- Work from home
Senior Trials Manager
University College London —London
- £54,931 - £64,644 a year
- Full-time
- Hybrid work
- Bachelor's degree
9d
Associate Professor in Implementation Science for Global Eye Health
London School of Hygiene & Tropical Medicine —London
- £64,469 - £73,994 a year
- Full-time
- Hybrid work
- Doctoral degree
- Annual leave
11d
Market Research Associate (Danish Speaking) - Remote
M3EU —London
- Full-time
- Remote
- English
- Microsoft Office
- Analysis skills
Quick apply
Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)
サイネオス・ヘルス —London
- Bachelor's degree
- Contracts
- Communication skills
Research Fellow in Computational Biology and AI
University College London —London
- £38,607 - £52,586 a year
- Full-time
- Hybrid work
- Doctoral degree
- C++
- Python
- Annual leave
- Employee assistance programme
12d
Clinical Lecturer/Clinical Associate Professor in Neuropathology
University College London —London
- £115,727 - £152,731 a year
- Full-time
- Doctoral degree
- Master's degree
- Teaching
- Annual leave
- Employee assistance programme
3d
Associate Director, Business Risk Lead (EU)
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Travel
Clinical Associate Professor in Spinal Surgery
Imperial College London —Hammersmith
- £113,565 - £150,569 a year
- Full-time
- Doctoral degree
- Rehabilitation centre
CRA II, client-dedicated (fixed-term)
Fortrea —Maidenhead
- Full-time
- Travel
- Organisational skills
- Communication skills
Clinical Data Strategy, Manager
Novartis —London
- £49,140 - £91,260 a year
- Full-time
- Hybrid work
Senior Health Economics and Outcomes Research Manager (Associate Director level)- 12 months Fixed-term contract
MSD —London
- Full-time
- Hybrid work
- Travel
8d
Trial Vendor Associate Director
Novartis —London
- £67,900 - £126,100 a year
- Full-time
- Hybrid work
- Communication skills
Associate Director, R&D Design Lead
Merck KGaA —London
- Doctoral degree
- English
- Master's degree
2d

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Senior CRA

ICON Plc -
Reading

Apply Now

Job details

Full-time

Benefits

Company pension
Employee assistance programme

Qualifications

Clinical research
Patient monitoring
Bachelor's degree
Communication skills

Full job description

Sr 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 - Clinical Research Associate (18 months' CRA experience required)

Location - must be based in the UK

Fully sponsor dedicated

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Key responsibilities include:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, 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
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Must have 4+ years' experience as a CRA to qualify for SCRA level
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex 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 .

Are you a current ICON Employee?

Apply Now

Refine Your Search

clinical research associate jobs in iver, bkm

Senior CRA

Clinical Trials Manager

Specialist, R&D Contracts & Business Operations

Associate Dean (Research and Innovation) - Faculty of Health and Medical Sciences

Research Fellow in Brain Vascular Biology and Brain Cancer Biology

Associate Director, Clinical Trial Lead (all genders)

Local Study Associate Director

Senior Trials Manager

Associate Professor in Implementation Science for Global Eye Health

Market Research Associate (Danish Speaking) - Remote

Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)

Research Fellow in Computational Biology and AI

Clinical Lecturer/Clinical Associate Professor in Neuropathology

Associate Director, Business Risk Lead (EU)

Clinical Associate Professor in Spinal Surgery

CRA II, client-dedicated (fixed-term)

Clinical Data Strategy, Manager

Senior Health Economics and Outcomes Research Manager (Associate Director level)- 12 months Fixed-term contract

Trial Vendor Associate Director

Associate Director, R&D Design Lead

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