Clinical research associates & coordinators Work, Jobs in Sandhurst, Ham (with Salaries)

Clinical Research Associate 1
ICON Plc —Reading
- Full-time
- Laboratory experience
- English
- Bachelor's degree
- Employee assistance programme
2d
Clinical Research Associate - IQVIA Biotech
IQVIA —Reading
- Full-time
- No degree
- Travel
- Recruiting
12d
Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Clinical Research Scientist
Montu UK —Winnersh
- £60,000 - £65,000 a year
- Part-time
- Hybrid work
- Analysis skills
- Project management
- Organisational skills
Quick apply
Clinical Research Associate I
Fortrea —Maidenhead
- Full-time
Clinical Registry Coordinator
ICON Plc —Reading
- Full-time
- Remote
- Project management
- Bachelor's degree
- Employee assistance programme
10d
Community Engagement Nurse (Private Practice Work in the Community)
CareForMe —Hounslow
- £30 an hour
- Part-time
- English
- In-person
- Communication skills
Quick apply
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Specialist Pharmacy Technician – Clinical Trials
Surrey and Borders Partnership NHS Foundation Trust —Chertsey
- £41,957 - £50,387 a year
- Part-time
- Travel
- Free parking
4d
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
- Travel
- Communication skills
CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- English
- Bachelor's degree
- Employee assistance programme
2d
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
Clinical Biospecimen Scientist - Single Sponsor Dedicated
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Work from home
Data Acquisition Specialist - External Data (Remote - UK)
IQVIA —Reading
- Full-time
- Remote
- Computer Science
- English
- Bachelor's degree
- Work from home
4d
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Data Team Lead
IQVIA —Reading
- Full-time
- Remote
- Oracle
- Bachelor's degree
- Leadership
- Work from home
3d
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Project management
- Work from home

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clinical research associates & coordinators jobs near sandhurst, ham

Clinical Research Associate 1

ICON Plc -
Reading

Apply Now

Job details

Full-time
2 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Laboratory experience
English
Bachelor's degree
Communication skills
FDA regulations

Full job description

CRA - In Vitro Diagnostics UK

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.

As a UK home-based In Vitro Diagnostics CRA at ICON, you will contribute to our clinical trial operations function, working in an enthusiastic, dynamic team.

This is a unique opportunity to move from a lab-based setting into a CRA role, embedded into a blue chip clinical diagnostics project, you will join your

colleagues in leading the design, planning, co-ordinating and conducting of all activities involved in initiating, monitoring and completing clinical research studies for in vitro diagnostics.

Responsibilities:

Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

ensuring studies are conducted according to study protocols, operating procedures, and good clinical practice.
validating product performance claims
supplying data for critical Regulatory submissions
defining the functional and clinical utility of investigation products
supplying data for critical Regulatory submissions
understanding and implementing federal regulations, helping to roll out SOPs in order to ensure that studies are adhering to FDA regulations, GCP, IVD directives and client policy.

Your Profile:

You will bring relevant In Vitro Diagnostics experience, ideally from a laboratory background, along with the following qualifications and skills.

Required qualifications and experience:

University degree in medicine, science, or equivalent
Practical knowledge of in vitro diagnostics and clinical trial processes
Excellent written and verbal communication in English
Good social skills enabling you to deal with queries in a timely manner
Willingness to travel as required from your UK base (occasionally internationally)

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 associates & coordinators jobs in sandhurst, ham

Clinical Research Associate 1

Clinical Research Associate - IQVIA Biotech

Clinical Research Associate II

Clinical Trial Associate

Clinical Research Scientist

Clinical Research Associate I

Clinical Registry Coordinator

Community Engagement Nurse (Private Practice Work in the Community)

Sr. Clinical Project Manager (Europe)

Specialist Pharmacy Technician – Clinical Trials

Manager, Clinical Study Lead

Clinical Trials Manager

Senior Clinical Trial Administrator

CRA

Senior CRA

Clinical Biospecimen Scientist - Single Sponsor Dedicated

Data Acquisition Specialist - External Data (Remote - UK)

Senior Clinical Programmer I

Data Team Lead

Local Study Associate Director

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