Iqvia uk Work, Jobs in London (with Salaries)

Clinical Research Associate, South East England
IQVIA —London
- Full-time
- Maintenance
- No degree
3d
Clinical Pharmacist
IQVIA —London
- Full-time
- Travel
- Annual leave
- Employee discount
Epidemiologist, Vaccines and Infectious Diseases (FSP Sponsor Dedicated)
IQVIA —London
- Full-time
- Remote
- Doctoral degree
- Master's degree
- Analysis skills
Urology Nurse - London
IQVIA —London
- Part-time
- Organisational skills
- Communication skills
Corporate Partnerships and Sponsorship Manager
IQVIA —London
- Full-time
- Business development
- Negotiation
Events and individual Giving Manager
IQVIA —London
- Full-time
- Project management
- Presentation skills
- Organisational skills
Key Account Manager
IQVIA —Reigate
- Full-time
- Sales
- Employee discount
- Gym membership
Pharmacy Business Manager
IQVIA —London
- Full-time
- Microsoft Powerpoint
- Sales
- Communication skills
- Annual leave
- Employee discount
12d
Clinical Project Manager
IQVIA —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
2d
Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)
IQVIA —London
- Full-time
- Remote
- Laboratory experience
- Project management
- Communication skills
42027- Associate Director Supplier Services
IQVIA —London
- Full-time
- English
- Project management
- IT
Sr RW Programmer/Sr Data Scientist/Analyst - Real World Data(US and UK Only)
サイネオス・ヘルス —London
- £80,600 - £145,000 a year
- English
- Master's degree
- SQL
- Employee stock purchase plan
- Annual leave
Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based
IQVIA —London
- Full-time
- Hybrid work
- Management
- Doctoral degree
- English
Senior Consultant and Statistician (Patient Centered Research) m/w/d
IQVIA —London
- Full-time
- Remote
- Doctoral degree
- Master's degree
- Communication skills
Senior Director, Product Management, Data Platforms & Analytics
IQVIA —London
- Full-time
- Doctoral degree
- Computer Science
- Engineering
6d
Senior Epidemiologist, Oncology (FSP Sponsor Dedicated)
IQVIA —London
- Full-time
- Remote
- Doctoral degree
- Data analysis skills
- Master's degree

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Clinical Research Associate, South East England

IQVIA -
London

Apply Now

Job details

Full-time
3 days ago

Qualifications

Clinical research
Maintenance

Full job description

London, United Kingdom | Full time | Field-based | R1550636

Join IQVIA on our mission to accelerate innovation for a healthier world!

IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South East England.

Why IQVIA?

Career development opportunities to grow as we grow
AI‑powered career advancement through our internal talent marketplace, Career Connections
Mentorship opportunities across the organisation via Employee Resource Groups
Flexible working to assist work–life balance and professional success
Well‑being support covering your physical, mental, and financial health

Awards

2026 "Glassdoor Best Place to Work in the UK"
#1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)
Brandon Hall Excellence Award for Learning & Development

Responsibilities

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
Collaborate and liaise with study team members for project execution support as appropriate

Requirements

Requires at least 6 months independent on-site monitoring experience of interventional studies
Experience across start-up, enrolment, maintenance, close-out
Digital literacy, including confidence using AI tools in a professional setting
Degree in scientific discipline / health care or equivalent industry experience
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Ability to establish and maintain effective working relationships with coworkers and clients
Full UK right to work required, this position is not eligible for visa sponsorship

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

#LI-ADAMTHOMPSON

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

Refine Your Search

iqvia uk jobs in london

Clinical Research Associate, South East England

Clinical Pharmacist

Epidemiologist, Vaccines and Infectious Diseases (FSP Sponsor Dedicated)

Urology Nurse - London

Corporate Partnerships and Sponsorship Manager

Events and individual Giving Manager

Key Account Manager

Pharmacy Business Manager

Clinical Project Manager

Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)

42027- Associate Director Supplier Services

Sr RW Programmer/Sr Data Scientist/Analyst - Real World Data(US and UK Only)

Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based

Senior Consultant and Statistician (Patient Centered Research) m/w/d

Senior Director, Product Management, Data Platforms & Analytics

Senior Epidemiologist, Oncology (FSP Sponsor Dedicated)

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