Research operations occupations Work, Jobs in Sherborne St. John, Ham (with Salaries)

Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
9d
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
6d
Research and Development Specialist
Tecna —Farnborough
- Up to £50,000 a year
- Full-time
- Hybrid work
- Data analysis skills
- Microsoft Office
- Project management
Quick apply
2d
Senior Impact Officer
University of Surrey —Guildford
- £37,694 - £42,254 a year
- Full-time
- Hybrid work
- University
- Organisational skills
- Communication skills
- Relocation assistance
- Annual leave
16h
Geoarchaeology Manager
Cotswold Archaeology —Andover
- £44,990 - £54,740 a year
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Access
- Annual leave
- Employee assistance programme
Quick apply
7d
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Part-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
8d
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
9d
CORDEX-IPO Programme Manager [26078]
HE Space —Didcot
- Full-time
- Hybrid work
- Doctoral degree
- English
- Master's degree
Quick apply
Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead
IQVIA —Reading
- English
- Microsoft Office
- Bachelor's degree
5d
Project Manager I, IDEA
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Communication skills
- Employee assistance programme
7d
Senior Study Start Up Associate
ICON Plc —Reading
- Full-time
- English
- Bachelor's degree
- Travel
- Employee assistance programme
8d
Digital Health Project Manager
ICON Plc —Reading
- Full-time
- Remote
- Management
- Project management
- Presentation skills
- Employee assistance programme
11h
Lead Business Operations Specialist
ICON Plc —Reading
- Full-time
- Patient monitoring
- Communication skills
- Employee assistance programme
2d
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
12d
Clinical Trial Manager - Project Lead
ICON Plc —Reading
- Full-time
- Oracle
- Management
- Project management
- Employee assistance programme
5d
Site Activation Specialist
IQVIA —Reading
- Remote
- Travel
- Contracts
- Negotiation
Clinical Supplies Project Manager
ICON Plc —Reading
- Full-time
- Management
- Project management
- Bachelor's degree
- Employee assistance programme
2d
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Associate Dean (Research and Innovation) - Faculty of Health and Medical Sciences
University of Surrey —Guildford
- Full-time
- University
9d

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research operations occupations jobs near sherborne st. john, ham

Senior CRA

ICON Plc -
Reading

Apply Now

Job details

Full-time
9 days ago

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

research operations occupations jobs in sherborne st. john, ham

Senior CRA

Study Start Up Associate

Research and Development Specialist

Senior Impact Officer

Geoarchaeology Manager

Sr. Clinical Project Manager (Europe)

Clinical Research Scientist

Clinical Trial Associate

CORDEX-IPO Programme Manager [26078]

Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead

Project Manager I, IDEA

Senior Study Start Up Associate

Digital Health Project Manager

Lead Business Operations Specialist

CRA

Clinical Trial Manager - Project Lead

Site Activation Specialist

Clinical Supplies Project Manager

Senior Clinical Programmer I

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

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