Trial associate Work, Jobs in Reading, Eng (with Salaries)

Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Microsoft Office
- Bachelor's degree
- Employee assistance programme
12d
Clinical Research Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
Study Start Up Associate II
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Travel
- Employee assistance programme
7d
Clinical Research Associate - 12 months' monitoring experience required
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
12d
Clinical Research Associate II
IQVIA —Reading
- Full-time
- No degree
Senior Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
8d
Patient Recruitment Associate II
ICON Plc —Reading
- Full-time
- Marketing
- Analysis skills
- Bachelor's degree
- Employee assistance programme
13d
Clinical Contracts Associate
ICON Plc —Reading
- Full-time
- Remote
- Master's degree
- Analysis skills
- Bachelor's degree
- Employee assistance programme
7d
Post-doctoral Research Associate / Research Trial Manager
Oxford Brookes University —Headington
- £36,636 - £39,906 a year
- Full-time
- Hybrid work
- Doctoral degree
- Supervising experience
- Project management
14d
CRA
ICON Plc —Reading
- Full-time
- Travel
- Communication skills
- Nursing
- Employee assistance programme
Research Facilitator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
11d
Payment Specialist
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Contracts
- In-person
- Annual leave
- Employee assistance programme
Senior Clinical Research Associate
IQVIA —Reading
- Full-time
- No degree
(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay
Moderna, Inc. —Oxford
- Overtime
- Microsoft Powerpoint
- Laboratory experience
- Master's degree
- Annual leave
8d
Associate Account Director, QualityMetric / Patient Centered Solutions (PCS)
IQVIA —Reading
- Full-time
- Sales
- Bachelor's degree
- Business
Senior CRA
ICON Plc —Reading
- Full-time
- Patient monitoring
- Bachelor's degree
- Travel
- Employee assistance programme
2d
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
1d
(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry
Moderna, Inc. —Oxford
- Full-time
- Laboratory experience
- Microsoft Office
- Presentation skills
- Annual leave
Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- Negotiation
Territory Manager, Vascular Access Management (VAM) - South West
BD —Winnersh
- £43,300 - £66,025 a year
- Sales
- Organisational skills
- IT

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trial associate jobs near reading, eng

Clinical Trial Associate

ICON Plc -
Reading

Apply Now

Job details

Full-time
12 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Clinical research
Microsoft Office
Bachelor's degree

Full job description

Cambridge (UK) Clinical Trial Associate to start ASAP!

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.

We are hiring a Clinical Trial Associate to start immediately or with 1 month notice maximum to join our dedicated team in Cambridge (England/UK).

You will have the opportunity to join a well-established team of dedicated CTAs providing key clinical trial administration support to exciting clinical trials. To succeed, you will demonstrate good UK clinical trial coordination with the ability to multi-task and work in fast-paced working environments.

The Role and Responsibilities

Responsible for study start-up activities, including creating site folders, collating, preparing and maintaining (e) SIP documents, updating systems
Liaise with clinical sites to collect, review and track feasibility questionnaires
Co-ordinates entry and maintain local data into study management systems (eClinical, CDSS/CDSSR, SADMS, etc.) including setting up new studies in eClinical
Ensures collection, review, track and provision of appropriate clinical documents to support regulatory submission and to perform IRB/IEC submissions including when appropriate preparation and submission of all documents to the central and/or local committee
Track and maintain adequate study related supplies in the office and facilitate their distribution to sites, including preparing and distributing Study File Binders, study drugs and Site Initiation
presentations/materials
Organise and participate in Investigator meetings and monitor workshops as required within budget guidelines
Processes, reconciles, distributes and tracks essential documents and submits them to RIM/EPIC or local archive in compliance with client’s SOPs
Orders, processes and tracks Case Report Forms (CRF) and follows up on query resolution
Manage local distribution of Investigator Brochure

Prepare and review site communication documents; facilitate mass mailings/faxes
Provide administrative support such as word processing, photocopying, faxing, filing, managing correspondence, presentations preparation, basic computer software support

Responsibilities:

Interacts with Clinical Research Services Manager for project or study related work
Supports the execution of clinical studies
Responsible for study start up activities
Tracks study related documents
Manages logistics and document exchange between clinical sites and the company
Actively contributes to results oriented department goals
Drives continuous improvement of GCSM
Promotes operational and scientific excellence within local GCSM
Identifies opportunities and best practices with local and regional partners that will contribute to overall operational effectiveness

What is Offered

Office-based 5 days per week in the Cambridge office (England/UK)
Full-time
Salary will be offered depending on the level of experience and skills
Permanent contract of employment with ICON and 100% dedicated to 1 single sponsor

What is required:

Ideally BA/BS/BSc or qualified nurse
UK-based clinical trial co-ordination/administration experience gained within the clinical research industry or within NHS trust/hospital setting

Proven ability to work efficiently and accurately with MS Office and EDC systems
Ability to work effectively within a fast-paced working environment using different electronic systems

Excellent and accurate attention to detail when entering data onto systems/database
Valid, current UK working eligibility

#LI-ET1

Onsite:#LI-Onsite

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

trial associate jobs in reading, eng

Clinical Trial Associate

Clinical Research Associate

Study Start Up Associate II

Clinical Research Associate - 12 months' monitoring experience required

Clinical Research Associate II

Senior Clinical Trial Associate

Patient Recruitment Associate II

Clinical Contracts Associate

Post-doctoral Research Associate / Research Trial Manager

CRA

Research Facilitator

Payment Specialist

Senior Clinical Research Associate

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

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

Senior CRA

Director, Portfolio Development Process & Standards Lead

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

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

Territory Manager, Vascular Access Management (VAM) - South West

I want to receive the latest job alerts for trial associate in reading, eng

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