4,224 Programming jobs in the United Kingdom
Statistical Programming (R Programming - Homebased)
Posted 13 days ago
Job Viewed
Job Description
**Responsibilities**
- Develop internal and external R packages for clinical trial analysis ( **ADaM, tables, figures, listings).**
- Validate **R packages.**
- **Lead implementation in R** and train other Biostatistics team members.
- Conduct statistical programming work of clinical data using R.
- Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group.
- Create and/or validate all safety and efficacy study output requirements (e.g. **ADaM, TLFs** ) consistent with data definitions and specifications and relevant study documentation (e.g. protocol, SAP, aCRF)
- Collaborates with peers and statisticians to ensure the quality and accuracy -thus submission readiness -of clinical data as required by authorities (i.e **. SDTM, ADaM, tables, figures, listings** , define.xml).
**Experience and Qualifications**
+ Minimum 5+ years of experience in R programming for clinical trial data including developing and validating R packages from CRO or Pharmaceutical Industry.
+ **Strong programming skills in R/R Shiny**
+ **Proven experience in applying R and R-Shiny for the analysis and reporting of clinical trials. Ability to reproduce statistical analysis using R.**
+ **Strong skills in data visualization and data wrangling using R. Proficiency in using R packages for data exploration and visualization.**
+ Application of statistical methodology and concepts in clinical trial analysis. Experience with R-Shiny apps for data exploration.
+ Advanced knowledge of industry standards including **CDISC** data structures as well as a solid understanding of the development and use of standard programs.
+ In-depth understanding of the phases of clinical trials and the drug development process.
+ Exposure to **Late Phase & Real-World Evidence (RWE)** studies is highly desirable.
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 is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Statistical Programming (R Programming - Homebased)
Posted 13 days ago
Job Viewed
Job Description
**Responsibilities**
- Develop internal and external R packages for clinical trial analysis ( **ADaM, tables, figures, listings).**
- Validate **R packages.**
- **Lead implementation in R** and train other Biostatistics team members.
- Conduct statistical programming work of clinical data using R.
- Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group.
- Create and/or validate all safety and efficacy study output requirements (e.g. **ADaM, TLFs** ) consistent with data definitions and specifications and relevant study documentation (e.g. protocol, SAP, aCRF)
- Collaborates with peers and statisticians to ensure the quality and accuracy -thus submission readiness -of clinical data as required by authorities (i.e **. SDTM, ADaM, tables, figures, listings** , define.xml).
**Experience and Qualifications**
+ Minimum 5+ years of experience in R programming for clinical trial data including developing and validating R packages from CRO or Pharmaceutical Industry.
+ **Strong programming skills in R/R Shiny**
+ **Proven experience in applying R and R-Shiny for the analysis and reporting of clinical trials. Ability to reproduce statistical analysis using R.**
+ **Strong skills in data visualization and data wrangling using R. Proficiency in using R packages for data exploration and visualization.**
+ Application of statistical methodology and concepts in clinical trial analysis. Experience with R-Shiny apps for data exploration.
+ Advanced knowledge of industry standards including **CDISC** data structures as well as a solid understanding of the development and use of standard programs.
+ In-depth understanding of the phases of clinical trials and the drug development process.
+ Exposure to **Late Phase & Real-World Evidence (RWE)** studies is highly desirable.
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 is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Statistical Programming (R Programming - Homebased)
Posted 13 days ago
Job Viewed
Job Description
**Responsibilities**
- Develop internal and external R packages for clinical trial analysis ( **ADaM, tables, figures, listings).**
- Validate **R packages.**
- **Lead implementation in R** and train other Biostatistics team members.
- Conduct statistical programming work of clinical data using R.
- Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group.
- Create and/or validate all safety and efficacy study output requirements (e.g. **ADaM, TLFs** ) consistent with data definitions and specifications and relevant study documentation (e.g. protocol, SAP, aCRF)
- Collaborates with peers and statisticians to ensure the quality and accuracy -thus submission readiness -of clinical data as required by authorities (i.e **. SDTM, ADaM, tables, figures, listings** , define.xml).
**Experience and Qualifications**
+ Minimum 5+ years of experience in R programming for clinical trial data including developing and validating R packages from CRO or Pharmaceutical Industry.
+ **Strong programming skills in R/R Shiny**
+ **Proven experience in applying R and R-Shiny for the analysis and reporting of clinical trials. Ability to reproduce statistical analysis using R.**
+ **Strong skills in data visualization and data wrangling using R. Proficiency in using R packages for data exploration and visualization.**
+ Application of statistical methodology and concepts in clinical trial analysis. Experience with R-Shiny apps for data exploration.
+ Advanced knowledge of industry standards including **CDISC** data structures as well as a solid understanding of the development and use of standard programs.
+ In-depth understanding of the phases of clinical trials and the drug development process.
+ Exposure to **Late Phase & Real-World Evidence (RWE)** studies is highly desirable.
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 is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Statistical Programming (R Programming - Homebased)
Posted 13 days ago
Job Viewed
Job Description
**Responsibilities**
- Develop internal and external R packages for clinical trial analysis ( **ADaM, tables, figures, listings).**
- Validate **R packages.**
- **Lead implementation in R** and train other Biostatistics team members.
- Conduct statistical programming work of clinical data using R.
- Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group.
- Create and/or validate all safety and efficacy study output requirements (e.g. **ADaM, TLFs** ) consistent with data definitions and specifications and relevant study documentation (e.g. protocol, SAP, aCRF)
- Collaborates with peers and statisticians to ensure the quality and accuracy -thus submission readiness -of clinical data as required by authorities (i.e **. SDTM, ADaM, tables, figures, listings** , define.xml).
**Experience and Qualifications**
+ Minimum 5+ years of experience in R programming for clinical trial data including developing and validating R packages from CRO or Pharmaceutical Industry.
+ **Strong programming skills in R/R Shiny**
+ **Proven experience in applying R and R-Shiny for the analysis and reporting of clinical trials. Ability to reproduce statistical analysis using R.**
+ **Strong skills in data visualization and data wrangling using R. Proficiency in using R packages for data exploration and visualization.**
+ Application of statistical methodology and concepts in clinical trial analysis. Experience with R-Shiny apps for data exploration.
+ Advanced knowledge of industry standards including **CDISC** data structures as well as a solid understanding of the development and use of standard programs.
+ In-depth understanding of the phases of clinical trials and the drug development process.
+ Exposure to **Late Phase & Real-World Evidence (RWE)** studies is highly desirable.
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 is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
R Programming Lead
Posted 13 days ago
Job Viewed
Job Description
**Responsibilities**
- Develop internal and external R packages for clinical trial analysis ( **ADaM, tables, figures, listings).**
- Validate **R packages.**
- **Lead implementation in R** and train other Biostatistics team members.
- Conduct statistical programming work of clinical data using R.
- Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group.
- Create and/or validate all safety and efficacy study output requirements (e.g. **ADaM, TLFs** ) consistent with data definitions and specifications and relevant study documentation (e.g. protocol, SAP, aCRF)
- Collaborates with peers and statisticians to ensure the quality and accuracy -thus submission readiness -of clinical data as required by authorities (i.e **. SDTM, ADaM, tables, figures, listings** , define.xml).
**Experience and Qualifications**
+ Minimum 5+ years of experience in R programming for clinical trial data including developing and validating R packages from CRO or Pharmaceutical Industry.
+ **Strong programming skills in R/R Shiny**
+ **Proven experience in applying R and R-Shiny for the analysis and reporting of clinical trials. Ability to reproduce statistical analysis using R.**
+ **Strong skills in data visualization and data wrangling using R. Proficiency in using R packages for data exploration and visualization.**
+ Application of statistical methodology and concepts in clinical trial analysis. Experience with R-Shiny apps for data exploration.
+ Advanced knowledge of industry standards including **CDISC** data structures as well as a solid understanding of the development and use of standard programs.
+ In-depth understanding of the phases of clinical trials and the drug development process.
+ Exposure to **Late Phase & Real-World Evidence** **(RWE)** studies is highly desirable.
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 is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
CNC Miller (Programming)
Posted 1 day ago
Job Viewed
Job Description
Below, you will find a complete breakdown of everything required of potential candidates, as well as how to apply Good luck.n£35,000 - £0,000 + Overtime (OTE 6,000) + Excellent Overtime Rates (up to 2x) + Half Day Friday + Days basednMotherwell
Are you a CNC miller with programming experience using Siemens, Fanuc, Mazatrol or Heidenhain controls looking for a stable role with a well-established company that offers the opportunity to massively boost your earnings through excellent overtime ra.
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Quality Inspector (CMM Programming)
Posted 14 days ago
Job Viewed
Job Description
Quality Inspector (CMM Programming)
35,000 - 40,000 + Days Based + Xmas Shutdown + Training and Development
Leighton Buzzard, Bedfordshire
Are you a Quality Inspector with a background in CMM Programming looking for a role where you'll have full responsibility for quality inspection for this busy machine shop?
Are you looking for an autonomous position, where you'll be recognised for your skill set as Chief Inspector?
In this role you will be working in a close partnership with the Quality Manager, covering all aspects of inspection and procedure. As a technical authority, you will be able to make improvements to processes. Day-to-day, you'll be a CMM and using hand-tools to inspect and measure parts.
This company create parts for many industries on short notice. They supply some of the biggest names in Oil & Gas, Automotive, Aerospace and the heavy engineering sectors. They have brilliant staff retention, enabling personal growth and career development.
This role would suit a Quality Inspector who can programme Co-ordinate Measurement Machines looking for an autonomous role that can offer responsibility and recognition as Chief Inspector.
The Role:
- Using CMM and Hand-Tools to inspect parts
- Driving Quality improvement with support from the Quality Manager
- Authority to create new processes
- Direct progression to Chief Inspector
- Monday - Thursday, 8am - 5pm, 2:30pm finish on Friday
The Person:
- Quality Inspector
- CMM Programming knowledge
Job Reference: BBBH 21452b
Quality, Inspector, ISO, 9001, AS, ISO9001, AS9100, 9100, CMM, Operator, Inspection, Engineer, Callipers, Gauges, Engineer, Manufacturing, CNC, Luton, Leighton Buzzard, Dunstable
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.
We are an equal opportunities employer and welcome applications from all suitable candidates. The salary advertised is a guideline for this position. The offered renumeration will be dependent on the extent of your experience, qualifications, and skill set.
Ernest Gordon Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job, you
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CNC Machinist (Milling / Programming)
Posted 14 days ago
Job Viewed
Job Description
CNC Machinist (Milling / Programming)
40,000 - 42,000 + Days Based + Monday to Friday + 33 Days Holiday + Overtime
Maidenhead
Are you a CNC Miller with programming experience looking for a long-term, stable role within a hugely successful, global manufacturer, working Monday to Friday and days only, with optional overtime to increase your earnings?
In this workshop-based role you will be working on a range of 3, 4, and 5 axis milling machines to produce components for a range of industries. You will be setting, operating, and programming the machines using Fanuc controls, with specific training given if needed.
Founded over 60 years ago, this manufacturer supplies specialist parts to the aerospace, automotive and motorsport industries globally, boasting continuous growth with a new site opened less than 2 years ago.
This role would suit a CNC Miller who can programme looking for a permanent, secure role with excellent working hours in a nice environment, promoting a healthy work-life balance.
The Role:
- Setting, operating, and programming CNC machines
- Using Fanuc controls with training given if needed
- Monday to Thursday, 8am - 4:30pm or 7am - 3:30pm, early finish on Fridays
- 19 - 20 an hour DOE
The Person:
- CNC Miller
- Can programme CNC machines
Reference: BBBH21693
Engineer, Engineering, CNC, Milling, Miller, Mill, Mills, Machine, Machinery, Computer, Setting, Setter, Operator, Programming, Programmer, Program, Slough, Reading, High Wycombe, Bracknell
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.
We are an equal opportunities employer and welcome applications from all suitable candidates. The salary advertised is a guideline for this position. The offered renumeration will be dependent on the extent of your experience, qualifications, and skill set.
Ernest Gordon Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job, you accept the T&C's, Privacy Policy and Disclaimers which can be found at our website.
Programming Trainee Placement Programme
Posted 14 days ago
Job Viewed
Job Description
*Please note this is a training programme with career placement and fees apply*
If you are looking to progress a career in computer programming or web development, then this training and placement programme is made for you?
Skills shortages in the IT sector are driving the need for qualified, entry-level career seekers and career changers.
All you need is a desire to work hard and invest some time and money in yourself to build the foundations for a new career.
We help you start your career journey in programming by firstly ensuring you have the necessary industry recognised certifications and skills required to build a career.
We ensure you market yourself properly through a structured career driven cv and LinkedIn profile highlighting your skills, any experience, and relevant transferable skills from other roles.
Finally, our tutors will help you create a credible portfolio to demonstrate your skills and abilities to potential new employers.
We have many years of experience in helping graduates find their first roles in top UK companies and organisations who need to employ entry-level qualified programming staff that can hit the ground running with up-to-date skills gained from this programme.
The programme is specifically designed for individuals with none or limited experience but a real desire to start a career. Therefore, please do not apply if you are already an experienced programmer.
Whether you are working full-time, part-time or are unemployed, this package has the flexibility to be completed at a pace that suits you and can be completed in as little as a few weeks or a few months (see steps 1 to 4 below). Study timings are approximate and assume you can study for a minimum 5 hours per week. *Training times will be reduced if you are able to invest more time each week.
Stage 1 – Learn HTML and CSS (*up to 12 weeks)
The first step is completing a selection of professional and industry-recognised courses. We have carefully selected these courses to give you the most out of both your learning and employment journey.
- HTML Essentials (*up to 6 weeks) li>CSS Essentials (*up to weeks)
Training is delivered through multimedia rich video tutorials, presentations and quizzes using an online portal enabling you to study online from anywhere you choose. You will also be assigned an expert tutor and a support mentor who will work with you 1-2-1 or in group sessions to provide additional training and support.
Once the HTML & CSS courses are complete, your trainer will move you forward to the next stage.
Stage 2 – Additional Online Training (*up to 12 weeks)
The second step includes a selection of more advanced courses to get you up to speed for what is required and relevant for many entry level programming roles and help you get a step ahead.
- < i>Learn the Command Line (*1.5 weeks)
- Learn Git & GitHub (*1.5 weeks)
- Learn JavaScript (*1.5 weeks)
- Learn Python 3 (*1.5 weeks)
JavaScript forms the foundation of almost everything you see on the Internet. Therefore, this is an essential addition language in building your programming and development foundation.
Python is a highly versatile programming language and due to its relatively “easy to understand” commands now one of the most common programming languages used. You can use it for both small and complex tasks, and it is used across many different industries broadening your scope of opportunity.
Step 3 - Building a Portfolio Website Project (1 week)
Your tutor will provide you with some exercises and guidelines to help you build your own personalised portfolio. Having a strong portfolio to which demonstrates and showcases your range of skills and ability is essential within a programming career.
In addition, we will now provide additional Study Courses for your continued development and broadening of your skills. Completion of these course is voluntary but recommended.
- Microsoft Certified: Azure Administrator Associate
Step 4 – Entry Level Coding placement
We will now work with you to help you secure your first role in a role utilising your new skills in a coding, programming, or web development role. There are many entry level roles where your newly learned skills can be applied meaning a vast array of opportunities are now available to you. Examples of some of these are listed below: -
- Website Support Developer
- Junior Web Developer
- Content Editor
- Wordpress Developer
- Junior Software Developer
- Junior Front or Back End Development
- Development Support
We have been helping career changers and new career seekers gain new careers since 2009 and we are a CompTIA Gold Partner, accredited by the BCS (Chartered Institute of IT/ British Computer Society) to ensure we provide the highest levels of training. We also have a 4.9 Trustpilot rating and numerous testimonials available on our website.
Our money back Job Guarantee
Due to our success and confidence in the results we deliver, and the skills shortage for entry-level coding staff we guarantee you will secure a job upon completion of your study programme, or we will refund you 100% of your course fees back. This is subject to our terms of learning/ terms of business.
Qualification for this programme?
To ensure we maintain a high level of support for our candidates, we limit spaces to this programme.
Apply before the deadline and one of our consultants will speak with you to check your eligibility for the programme.
Quality Inspector (CMM Programming)
Posted 2 days ago
Job Viewed
Job Description
Quality Inspector (CMM Programming)
35,000 - 40,000 + Days Based + Xmas Shutdown + Training and Development
Leighton Buzzard, Bedfordshire
Are you a Quality Inspector with a background in CMM Programming looking for a role where you'll have full responsibility for quality inspection for this busy machine shop?
Are you looking for an autonomous position, where you'll be recognised for your skill set as Chief Inspector?
In this role you will be working in a close partnership with the Quality Manager, covering all aspects of inspection and procedure. As a technical authority, you will be able to make improvements to processes. Day-to-day, you'll be a CMM and using hand-tools to inspect and measure parts.
This company create parts for many industries on short notice. They supply some of the biggest names in Oil & Gas, Automotive, Aerospace and the heavy engineering sectors. They have brilliant staff retention, enabling personal growth and career development.
This role would suit a Quality Inspector who can programme Co-ordinate Measurement Machines looking for an autonomous role that can offer responsibility and recognition as Chief Inspector.
The Role:
- Using CMM and Hand-Tools to inspect parts
- Driving Quality improvement with support from the Quality Manager
- Authority to create new processes
- Direct progression to Chief Inspector
- Monday - Thursday, 8am - 5pm, 2:30pm finish on Friday
The Person:
- Quality Inspector
- CMM Programming knowledge
Job Reference: BBBH 21452b
Quality, Inspector, ISO, 9001, AS, ISO9001, AS9100, 9100, CMM, Operator, Inspection, Engineer, Callipers, Gauges, Engineer, Manufacturing, CNC, Luton, Leighton Buzzard, Dunstable
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.
We are an equal opportunities employer and welcome applications from all suitable candidates. The salary advertised is a guideline for this position. The offered renumeration will be dependent on the extent of your experience, qualifications, and skill set.
Ernest Gordon Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job, you