Clinical associate Work, Jobs in Newbury, Brk (with Salaries)

Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
- Employee assistance programme
2d
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 Contracts Associate
ICON Plc —Reading
- Full-time
- Remote
- Master's degree
- Analysis skills
- Bachelor's degree
- Employee assistance programme
10d
(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay
Moderna, Inc. —Oxford
- Overtime
- Microsoft Powerpoint
- Laboratory experience
- Master's degree
- Annual leave
10d
Clinical Research Associate - 12 months' monitoring experience required
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
14d
Research Facilitator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
13d
(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry
Moderna, Inc. —Oxford
- Full-time
- Laboratory experience
- Microsoft Office
- Presentation skills
- Annual leave
RWE Associate Clinical Project Manager – Oncology (FSP)
IQVIA —Reading
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
6h
Senior Associate Physiotherapist
Therapies On Thames —Newbury
- £45 - £50 an hour
- Part-time
- Anatomy knowledge
- Patient care
- Medical terminology
Quick apply
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Patient Recruitment Associate II
ICON Plc —Reading
- Full-time
- Marketing
- Analysis skills
- Bachelor's degree
- Employee assistance programme
Senior Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
10d
Manager - Patient Experience Data
IQVIA —Reading
- Full-time
- Remote
- Project management
- IT
- Time management
4d
Overseas Patients Co-ordinator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
- Administrative experience
- Communication skills
Hospital Pharmacy Workflow Specialist - Plymouth
BD —Winnersh
- £42,000 - £64,050 a year
- Full-time
- Hybrid work
- Hospital
- Travel
- In-person
Regulatory Science and Policy Associate - VIE Contract
Sanofi —Reading
- English
- Communication skills
15h
Associate Clinical Psychologist
Well Mind People Ltd —Wallingford
- £60 - £70 an hour
- Childcare
- Working with children
- Bachelor's degree
Quick apply
8d
Clinical Post Market Surveillance Sr Specialist
Zimmer Biomet —Swindon
- Full-time
- Analysis skills
- Travel
- Health & wellbeing programme
Research Associate in Neural Rendering and Medical Image Reconstruction
University of Oxford —Oxford
- £39,424 - £43,984 a year
- Doctoral degree
- Machine learning
- In-person
- Annual leave

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Clinical Trial Associate

ICON Plc -
Reading

Apply Now

Job details

Full-time
2 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Clinical research
Bachelor's degree
Organisational skills
Communication skills

Full job description

Clinical Trial Administrator - 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.

Here at the ICON FSP group, we are in partnership with one of the world’s leading Independent Biotechnology companies and we’re looking for experienced, UK-based Clinical Research Administrators to commit to a hybrid home and office-based environment in Luton, England.

We're looking for experienced candidates with a good understanding of clinical trial documentation processes, and a good general understanding of the responsibilities of a CTA.

As a guide, you will need to demonstrate coordination and administration of study activities from the start up to execution and close out on a handful of clinical projects. A more detailed job description and benefits list will be shared with you at a later time-point.

These are full-time, permanent roles, with real development opportunities and an exciting and rewarding portfolio of work for successful candidates.

Responsibilities

Assist in the coordination and administration of a variety of clinical trials, ensuring compliance with protocols and regulatory requirements.
Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
Support the preparation of study-related materials, such as informed consent forms and case report forms.
Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
Contribute to the tracking and reporting of clinical trial metrics and milestones.

Your profile

Bachelor's degree in a scientific or healthcare-related field.
Prior experience or strong interest in clinical research.
Knowledge of clinical trial processes, regulations, and guidelines.
Excellent organizational and communication skills.
Ability to work collaboratively in a fast-paced environment with attention to detail.

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 associate jobs in newbury, brk

Clinical Trial Associate

Clinical Research Associate

Clinical Research Associate II

Clinical Contracts Associate

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

Clinical Research Associate - 12 months' monitoring experience required

Research Facilitator

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

RWE Associate Clinical Project Manager – Oncology (FSP)

Senior Associate Physiotherapist

Senior Clinical Research Associate

Patient Recruitment Associate II

Senior Clinical Trial Associate

Manager - Patient Experience Data

Overseas Patients Co-ordinator

Hospital Pharmacy Workflow Specialist - Plymouth

Regulatory Science and Policy Associate - VIE Contract

Associate Clinical Psychologist

Clinical Post Market Surveillance Sr Specialist

Research Associate in Neural Rendering and Medical Image Reconstruction

I want to receive the latest job alerts for clinical associate in newbury, brk

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