Clinical trial associate Work, Jobs in Mortimer Common, Ham (with Salaries)

Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
- Employee assistance programme
1d
Clinical Trial Assistant -Base
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
14h
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 Associate - 12 months' monitoring experience required
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
13d
Clinical Contracts Associate
ICON Plc —Reading
- Full-time
- Remote
- Master's degree
- Analysis skills
- Bachelor's degree
- Employee assistance programme
9d
Senior Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
9d
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
Research Facilitator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
13d
Study Start Up Associate II
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Travel
- Employee assistance programme
8d
Patient Recruitment Associate II
ICON Plc —Reading
- Full-time
- Marketing
- Analysis skills
- Bachelor's degree
- Employee assistance programme
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
Payment Specialist
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Contracts
- In-person
- Annual leave
- Employee assistance programme
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
3d
Director, Portfolio Development Process & Standards Lead
CSL Behring —Maidenhead
- £250,000 - £280,000 a year
- Full-time
- Hybrid work
- Nursing
- Master's degree
- Bachelor's degree
3d
Sr CRA - Oncology experienced required
ICON Plc —Reading
- Full-time
- Programmable logic controllers
- Travel
- Communication skills
- Employee assistance programme
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- Negotiation
Associate Country Clinical Quality Manager
Fortrea —Maidenhead
- Full-time
- Analysis skills
- Bachelor's degree
Associate Account Director, QualityMetric / Patient Centered Solutions (PCS)
IQVIA —Reading
- Full-time
- Sales
- Bachelor's degree
- Business
Territory Manager - North West
BD —Winnersh
- £43,300 - £66,025 a year
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
10d

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clinical trial associate jobs near mortimer common, ham

Clinical Trial Associate

ICON Plc -
Reading

Apply Now

Job details

Full-time
1 day 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 trial associate jobs in mortimer common, ham

Clinical Trial Associate

Clinical Trial Assistant -Base

Clinical Research Associate

Clinical Research Associate II

Clinical Research Associate - 12 months' monitoring experience required

Clinical Contracts Associate

Senior Clinical Trial Associate

Senior Clinical Research Associate

Research Facilitator

Study Start Up Associate II

Patient Recruitment Associate II

CRA

Payment Specialist

Senior CRA

Director, Portfolio Development Process & Standards Lead

Sr CRA - Oncology experienced required

Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)

Associate Country Clinical Quality Manager

Associate Account Director, QualityMetric / Patient Centered Solutions (PCS)

Territory Manager - North West

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