JUMP TO CONTENT

Software Engineer / Web developer (PHP)

055483_2

About the role

This vacancy has now expired. Please click here to view live vacancies.

ICON’s Patient Centered Services (PCS) group is looking for a UK-based PHP developer to join our team. Our team develops and maintains a suite of applications for use by the staff, customers, and suppliers of the PCS group, covering areas such as project management, customer requests, supplier invoicing, and integration with other tools used by the business.


What you’d get from ICON

  • The choice of full-time working from home or a desk in our office in Milton Park, Oxfordshire.
  • Flexible working hours: quality and consistency of output are more important to us than clocking in at 9am and out at 5pm.
  • Work on long-term bespoke software projects. You’ll have a major input into the design and architecture of all of PCS’ software projects.
  • Have the opportunity to have a say in the technical direction of the PCS group.
  • Support to develop your technical skills and interests.
  • The chance to attend relevant industry conferences and workshops.

What we need from you:


Demonstrable experience working in web development in a professional environment, ideally with a focus on PHP


Experience in all of the following areas:

  • Written & spoken English
  • Object-oriented PHP
  • Modern JavaScript
  • Testing including Test-Driven Development (TDD)
  • Commercial awareness and experience in using technology to solve real business problems
  • Independence and self-sufficiency
  • Web technologies such as HTTP, APIs, HTML, AJAX, CSS, etc.
  • Relational databases including MySQL
  • Git

Knowledge of the following tools/frameworks would be beneficial but is not essential:

  • CakePHP
  • Laravel
  • VueJS

About ICON


ICON Clinical Research is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialise in the strategic development, management and analysis of programs that support Clinical Development - from compound selection to Phase I-IV clinical studies.


ICON Patient Centred Sciences comprises expertise spanning four decades of innovation and research on directly engaging with patients across the entire healthcare landscape and through the entire treatment lifecycle. Bringing together expertise from staff around the world, we deliver a full service approach to patient centred outcomes, including the development, validation, licensing, translation, cultural validation and analysis of patient reported outcomes (PROs). The PCS development team develops and maintains software solutions to help support the business.


About you

  • You have demonstrable experience of working on web-based applications in a commercial environment, possibly in a variety of roles in the software development industry.
  • You are driven to develop your own skills and stay up-to-date.
  • You are a good communicator, especially with non-technical people.
  • You have access to previous examples of your work and are willing for us to approach previous employers or clients for testimonials/references.
  • Home-based only: you have a private, dedicated home-working space, you live in the UK and are able to travel to our Milton Park office a couple of times a year

If this sounds like you, we’d love to hear from you.

List #1

Day in the life

Headshot of male
Leading Through Change: Zhong Yao's Journey at ICON in China

Teaser label

Our People

Content type

Blogs

Publish date

12/10/2025

Summary

Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.

Teaser label

From culture to collaboration, Zhong Yao explains how ICON China delivers quality clinical trials, and empowers local talent.

Read more
Two computer monitors with data graphs
How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish date

12/01/2025

Summary

How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i

Teaser label

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

Read more
Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish date

11/28/2025

Summary

Quality and Compliance for New Entrants:           A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

Read more
View all

Similar jobs at ICON

Senior CRA

Salary

Location

Poland, Warsaw

Location

Warsaw

Gdansk

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Contractor

Description

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical

Reference

JR140767

Expiry date

01/01/0001

Michal Czyrek

Author

Michal Czyrek
Read more Shortlist Save this role
Senior Manager, Clinical Operations, Diagnostics

Salary

Location

US, Blue Bell (ICON)

Location

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Operations Management

Job Type

Permanent

Description

We are currently seeking a Senior Manager, Clinical Operations to join our diverse and dynamic team who has a Lab background or experience in diagnostics. As a Senior Manager, Clinical Operations at I

Reference

JR140902

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
Clinical Research Associate - Oncology experience required

Salary

Location

UK, Reading

Location

Reading

Remote Working

Office or Home

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Role: Clinical Research Associate (CRO and/or Pharma monitoring and Oncology experience required) Location: Must be based in the UK, nationwide travel  Fully sponsor dedicatedAs a CRA you will be joi

Reference

JR140245

Expiry date

01/01/0001

Amani Yousef

Author

Amani Yousef
Read more Shortlist Save this role
Logistics Specialist

Salary

Location

Ukraine, Kyiv IKBP

Department

Full Service - Global Logistics

Location

Kiev

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Supplies

Job Type

Permanent

Description

We are currently seeking a Logistics Specialist to join our diverse and dynamic team in Ukraine. As a Logistics Specialist you will play a vital role by managing the end-to-end logistics process. This

Reference

JR134661

Expiry date

01/01/0001

Salome Kankia

Author

Salome Kankia
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

United States of America

Location

Multiple US Locations

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical

Reference

JR140876

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Cardiac Data Processing Specialist

Salary

Location

India, Chennai

Department

Full Service - Development & Commercialisation Solutions

Location

Chennai

Trivandrum

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Data Management

Job Type

Permanent

Description

.The Cardiac Data Processing Specialist is responsible for data review, quality assurance, and data correction according to predefined study-specific specifications. Origins of data that may be includ

Reference

JR140799

Expiry date

01/01/0001

Sunidhi Sinha

Author

Sunidhi Sinha
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above