Clinical trial administrator Work, Jobs in Reading, Brk (with Salaries)

Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
- Employee assistance programme
2d
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
- Travel
- Communication skills
11d
Agile Research Delivery Team Administrator B4
Royal Surrey NHS Foundation Trust —Guildford
- £29,812 - £32,715 a year
- Full-time
- IT
8d
Graduate Studies Administrator
University of Oxford —Oxford
- £32,108 - £37,338 a year
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
1d

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Clinical Trial Associate
ICON Plc —Reading
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…
2d
Clinical Research Associate
ICON Plc —Reading
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.

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Clinical Trial Associate

ICON Plc -
Reading

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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

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clinical trial administrator jobs in reading, brk

Clinical Trial Associate

Senior Clinical Trial Administrator

Agile Research Delivery Team Administrator B4

Graduate Studies Administrator

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