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Join Our Team as a Senior Clinical Statistical Programmer!\n Are you ready to take your programming skills to the next level? At CSL, we’re on the lookout for a Senior Programmer who will take technical ownership of one or two clinical trials, guiding them from the first line of code to the final submission package. This is not just any programming role; it’s a hands-on position where your expertise will be crucial in ensuring the integrity of clinical data. Why This Role Matters\n In the world of clinical trials, trustworthy programming is essential. Every regulatory decision—whether a safety signal is caught or missed—depends on the quality of the datasets and outputs. As a Senior Programmer, you’ll be at the heart of this process, shaping how analyses are structured and ensuring they are submission-ready. You won’t just execute specifications; you’ll often be the one writing them, catching ambiguities before they become issues. Your Responsibilities\n As the lead programmer for your assigned studies, you will: \n\n • Interpret protocols, SAPs, data management plans, and CRF specifications to drive study setup and analysis.\n, • Design and validate SDTM and ADaM datasets, tables, figures, and listings in collaboration with study statisticians.\n, • Review and take ownership of CRO-produced deliverables, ensuring they meet submission-ready quality standards.\n, • Lead the specification and delivery of integrated analyses (e.g., ISS/ISE) and associated outputs when not handled by a CRO.\n, • Mentor less experienced programmers on internal processes and standards, contributing to departmental tools and process improvements.\n, • Engage in ad hoc analytical work, including regulatory query responses, exploratory analyses, and publication support as needed.\nWhat We’re Looking For\n To thrive in this role, you should have: \n\n • Experience in programming within pharmaceutical, biotech, CRO, or clinical research settings.\n, • Strong proficiency in SAS (Base/Macro/Stat/Graph); familiarity with R or other programming languages is a plus.\n, • A working knowledge of current CDISC standards — CDASH, SDTM, ADaM, define.xml.\n, • A proven track record of producing and validating submission-ready TFLs and datasets, including ad hoc analytical requests.\n, • Experience supporting regulatory submissions (FDA required; PMDA, NMPA, or EMA experience is a bonus).\n, • Comfort in working with external vendors and CRO-managed data.\n, • A BSc in Computer Science, Mathematics, Statistics, or a related field; equivalent experience and certifications will also be considered.\nWorking Conditions\n This position is hybrid-based, requiring you to be onsite in Maidenhead for three days a week. Enjoy the flexibility of working from home while still being part of a collaborative team environment! Why Join Us?\n At CSL, we believe in the power of our people. By joining our team, you’ll not only contribute to groundbreaking clinical trials but also have opportunities for professional growth and development. We value your expertise and are committed to supporting your career journey. \n If you’re ready to make a significant impact in the world of clinical programming, we’d love to hear from you!

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ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are seeking an experienced Pharmacometrics Support Programmer to join a global FSP team. This is an opportunity for a highly analytical programmer with strong R programming expertise and experience in PK/PD data preparation to contribute to critical drug development programmes. In this role, you will be responsible for the creation, quality control, and standardisation of NONMEM PK/PD datasets, supporting pharmacometric modelling activities across a diverse clinical portfolio. Working closely with Data Management, Statistical Programming, Statistics, Bioanalytical teams, and external partners, you will play a key role in ensuring high-quality pharmacometric data is delivered on time and to the highest regulatory standards. • Develop and quality control NONMEM PK/PD datasets using SDTM and ADaM data sources., • Support pharmacometric modelling activities by delivering accurate, complete, and submission-ready datasets., • Perform quality review of internally and externally produced NONMEM datasets., • Collaborate with Data Management, Statistical Programming, Statistics, Clinical Pharmacology, and Bioanalytical teams to resolve data issues and ensure project timelines are met., • Contribute to the preparation of regulatory submission projects in accordance with internal pharmacometrics guidelines., • Conduct quality control testing of customised R packages used to standardise pharmacometric workflows., • Develop and maintain testing frameworks and validation processes for departmental R tools and packages., • Identify data discrepancies, process improvements, and opportunities for greater automation and efficiency., • Actively contribute to the development and implementation of new pharmacometric standardisation initiatives., • Ensure all deliverables comply with applicable SOPs, working instructions, regulatory requirements, and ICH-GCP guidelines., • Maintain inspection readiness through ongoing training and adherence to quality standards., • Bachelor's degree in a Life Science, Health Science, Statistics, Computer Science, IT, or related discipline., • Minimum of 6 years' experience within the pharmaceutical, biotechnology, or CRO industry., • Strong programming expertise in R., • Experience developing and quality controlling NONMEM PK/PD datasets., • Working knowledge of PK/PD principles and pharmacometric workflows., • Strong understanding of SDTM, ADaM, and CDISC standards, including controlled terminology., • Experience supporting NONMEM file creation, quality control, submissions, and standardisation activities., • Strong attention to detail and commitment to data quality., • Excellent written and verbal communication skills in English., • Experience reviewing and managing outsourced programming deliverables., • Experience validating or quality controlling customised R packages., • Demonstrated ability to identify process improvements and drive standardisation initiatives., • Ability to work effectively across global, cross-functional teams., • Opportunity to work within a globally recognised Clinical Pharmacology & Pharmacometrics function., • Contribute directly to innovative drug development programmes., • Work in a highly collaborative and scientifically driven environment., • Be part of ongoing innovation and standardisation initiatives within pharmacometrics and clinical data science., • Use your expertise to influence best practices and improve the efficiency and quality of pharmacometric deliverables. If you are passionate about leveraging R programming, pharmacometrics, and data quality excellence to support drug development, we'd love to hear from you. Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. • Various annual leave entitlements, • A range of health insurance offerings to suit you and your family’s needs., • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead., • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being., • Life assurance, • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. #J-18808-Ljbffr

ICON plc is a world-leading healthcare intelligence and clinical research organisation seeking an experienced Pharmacometrics Support Programmer. The role focuses on R programming and PK/PD data preparation to support critical drug development programmes. You will create, QC and standardise NONMEM PK/PD datasets, collaborate across Data Management, Statistics and Bioanalytical teams, and contribute to regulatory submissions with a focus on quality and timeliness. #J-18808-Ljbffr

(Tech stack: .NET Developer, .NET 10.0, ASP.NET Core, C# 14, .NET MAUI, ML.NET, Azure AI, GitHub Copilot, Docker, Kubernetes, .NET Aspire, CI/CD, HTML Living Standard, CSS Living Standard, Programmer, Full Stack Engineer, Architect, .NET Developer) Our client has long been a classic internet icon; today it has evolved into an integrated and diversified modern media company. We are seeking .NET Developer to work on one of the most ambitious .NET / C# projects to take place since the birth of the World Wide Web. .NET Developer applicants should have a skill set that encompasses: • .NET, • .NET Core, • C#, • Azure SQL Full training will be provided into: • .NET 10.0, • C# 14, • .NET MAUI, • ML.NET, • Azure AI, • GitHub Copilot, • Docker, • Kubernetes, • .NET Aspire, • CI/CD, • HTML Living Standard, • CSS Living Standard, • Azure, • Azure Cosmos DB Our client offers a truly refreshing working environment: • flexible working hours, • home working, • casual dress code, • onsite gym, • games room, • great benefits This is an amazing opportunity to join a major force in the Internet arena industry, with a proud heritage, an enduring legacy and a promising future. Applicants must be based in the UK and have the right to work in the UK even though remote working is available. #J-18808-Ljbffr

Possible Location: UK, Spain, Belgium, South Africa, Romania, Hungary, Ireland, France, Italy, Czech Republic, Bulgaria. This unique role within IQVIA is ideal for someone with a technical mindset, strong communication skills, and a good understanding of SDTM. Experience in Study Design, CRF annotation, CDISC standards, and vendor management will be key for success in this position. The role can be performed remotely from a number of countries in Europe or South Africa. As part of a dedicated sponsor team, you will work directly with the client to manage database and CRF-related activities while overseeing SDTM deliverables throughout the study lifecycle. The primary responsibility of this role is to provide end-to-end oversight of SDTM activities. This includes managing CRF design based on study protocols, ensuring vendor specifications align with SDTM requirements, contributing to SDTM specifications when required, and performing SDTM review and oversight to ensure the quality, consistency, and completeness of SDTM datasets and deliverables. • Collaborate with Sponsor colleagues and CRO Partners to review CRF design and compliance into standard and SDTM., • In collaboration with Study Data Leads ensure the planning for data receipt and its oversight throughout the duration of assigned clinical trials, • Program reports and contribute to the standardization of process and reports used for data review and analysis for external partners/vendors and internal teams, • Complete formal and ad-hoc analyses and oversight of SDTM data., • Review of critical document/deliverable (SDTM Annotation, SDTM datasets) to ensure Data Standards are used consistently and support creation of DE dataset, • Map SDTM data and manage annotated CRF, • Attend meetings as applicable with Mission, Submission, Project, Program, JCST, DEM, Biometrics, Clinical & Regulatory Solutions Team (CRST), Early Phase, • Perform relevant quality checks and create standard edit checks for new CRF modules and share in the appropriate space, • Support audits and inspections as required and other responsibilities and projects that the Company may assign., • At least 5 years relevant in either SDTM oversight and/or CRF design, • Experience with Biometrics processes to include:, • Review of SDTM annotated CRFs, • Writing and reviewing technical specifications, • Review of log files for errors and warnings, • Resolving/trouble shooting errors, • Experience with data mapping and SDTM Controlled Terminology, • Experience with SAS programming and SDTM deliveries is an added value, • Prior experience in a clinical or pharmaceutical related field is required., • Prior experience in a Data Management related field is required, • Experience with relational databases, preferably Clinical Data Management and EDC Systems, • Advanced familiarity with reporting tools., • Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices., • Excellent command, both verbal and written, of English 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 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. #J-18808-Ljbffr

Job Title: Game Design Tutor Location: Reading Salary: Starting from £25,000 per annum Job type: Fixed Term, Full Time. Start Date: Immediate. Enemy of Boredom (EOB) is a video game design training centre working with young people with Special Educational Needs and Disabilities (SEND) to build futures. We are the academy of creative excellence for young people who think differently, delivering contemporary arts education and alternative provision through video games design, music performance and preparing-for-adulthood life skills courses. We are seeking a passionate and creative Game Design Tutor to join our team at our Reading studio , delivering Level 1, 2 and 3 video game design courses to young people with SEND. The Role: As a Game Design Tutor, your task is to equip neurodivergent young people with the video game design skills needed to create a more beautiful digital world. Working both online and in person, you will offer students opportunities to develop their skills, confidence and capabilities through learning video game design - education without boundaries . You will plan and deliver engaging, well-structured lessons and workshops, adapting your teaching to meet the individual strengths and needs of your students. You will work closely with students to support their development, monitor progress and contribute to their wider educational outcomes, including relevant EHCP targets. This is an exciting opportunity for someone who is passionate about video games, creative education and supporting young people to achieve their potential. Skills and Abilities That EOB Look For: You need to be trained to degree level in video game-related courses or have relevant industry experience. Current teaching qualification or willingness to take one on. A keen interest in pop culture and a passion for the games industry. The ability to understand young people and their differences when learning, helping to promote growth and confidence. Comfortable working in the venue as well as online with students. A genuine enjoyment of lesson and workshop planning. The ability to report and record data and progress accurately. Self-motivated and able to contribute ideas for continuous improvement. Solid organisational skills and the ability to adapt and be flexible to tasks. A passion for helping young people with SEND develop their creative and digital skills. Duties and Responsibilities: Teaching: Plan and teach well-structured lessons to assigned classes, following EOB's plans, curriculum and schemes of work. Deliver engaging Level 1, 2 and 3 video game design sessions. Assess, monitor, record and report on the learning needs, progress and achievements of assigned pupils, making accurate and productive use of assessment. Adapt teaching to respond to the strengths and needs of pupils. Set high expectations which inspire, motivate and challenge pupils. Promote good progress and outcomes by pupils. Demonstrate good subject and curriculum knowledge. Run EHCPs relevant to your students. Participate in arrangements for preparing pupils for external tests. Plan practical workshops and activities that develop students' technical and creative skills. Support students to develop their confidence, independence and understanding of the wider games industry. Safeguarding, Health & Safety: Follow safeguarding policies and report any concerns immediately in line with procedure. Support online safety practices where delivery includes digital platforms. Adhere to health and safety guidance, including risk assessments for practical activities. Maintain appropriate professional boundaries with students at all times. Contribute to a safe, inclusive and positive learning environment. About You: You will be creative, enthusiastic and passionate about video game design and education. You will understand that young people learn in different ways and will be able to adapt your approach to help individual students engage, develop and succeed. You will also be organised and reliable, with the ability to plan effectively, maintain accurate records and work collaboratively with colleagues. Experience working with young people with SEND would be advantageous, as would knowledge of relevant creative software and game development platforms. What We Offer: 45 days' holiday, to be taken in line with the school's holiday calendar and subject to you being up to date with planning, marking, assessment requirements and associated admin for your role. Confidential support through an Employee Assistance Programme (EAP). Stress management and wellbeing resources. Flexible working arrangements where the role allows. Paid day off for your birthday. Team and social activities. The opportunity to work in a creative and supportive environment focused on helping young people succeed. Candidates with the relevant experience or job titles of Games Designer, Games Animator, Computer Animation, Games Artist, Video Game Programmer, Video Game Developer, Graphic Designer, Interactive Media Designer, Digital Artist or similar may also be considered for this role. TPBN1_UKTJ

IQVIA LLC in Reading, United Kingdom, seeks an experienced PK/PD Statistical Programmer to join our pharmacometrics team. You will program, validate, and deliver NONMEM-ready PK/PD datasets based on SDTM/ADaM standards using advanced R skills, ensuring accuracy from unclean to post‑lock clinical data. The role requires 6+ years in clinical data analysis or pharmacometrics, expert R proficiency, and hands-on NONMEM dataset creation. #J-18808-Ljbffr

Senior Clinical Statistical Programmer (Portfolio Development / Biometrics / Programming). This is a hands-on statistical programming role with real authority attached to it: you'll be the person a study team turns to when the data needs to hol.

IQVIA is seeking an experienced Statistical Programmer to develop and coordinate programming for the full spectrum of statistical deliverables. You will plan, execute, and validate complex analyses, and collaborate with internal and external clients to meet study objectives. The role requires strong SAS/ADaM skills, CDISC experience, and the ability to lead projects and train junior staff. Based in Reading, the position is full-time with opportunities to impact multiple studies. #J-18808-Ljbffr

ICON Strategic Solutions seeks an experienced Pharmacometrics Support Programmer to join a global FSP team in Reading, UK.

We are seeking an experienced Pharmacometrics Support Programmer to join a global FSP team. This is an opportunity for a highly analytical programmer with strong R programming expertise and experience in PK/PD data preparation to contribute to critical drug development programmes.

Reading, Berkshire, United Kingdom.This role supports Pharmacometrics by producing high‑quality, compliant datasets for modeling and analysis, ensuring accuracy from early (unclean) through post‑lock clinical data.The ideal candidate brings deep technical expertise, strong problem‑solving skil

IQVIA in Reading, UK seeks an experienced PK/PD Statistical Programmer to support pharmacometrics by producing high-quality NONMEM-ready PK/PD datasets using SDTM/ADaM standards.

Seeking an Oracle Programmer with expertise in Oracle Commerce to design, develop, and maintain Oracle-based solutions, writing PL/SQL code and collaborating on technical requirements.

Sit on the internal Design Authority Board (DAB) and review proposed designs to ensure compliance with the agreed terms of reference for Targets technical strategy. Play a key role in Targets modernisation by utilising your skills and knowledge of the IT industry to shape solutions. Research, invest

AI Trainee Engineer – £45,000–£75,000 – Job Programme \n Looking to start a career in AI Engineering? \n We are offering a structured pathway into AI Engineering, designed to help you enter one of the fastest-growing sectors in tech with no prior experience.This opportunity includes traini

Are you a Sliding Head CNC Programmer or Machinist looking for an exciting next step in your career, working with highly bespoke CNC Lathes for an OEM, that will encourage your development through tailored in-house training, enabling you to become a fully-fledged Applications Engineer?. This role wo

AI Trainee Engineer – £45,000–£75,000 – Job Programme \n Looking to start a career in AI Engineering? \n We are offering a structured pathway into AI Engineering, designed to help you enter one of the fastest-growing sectors in tech with no prior experience.This opportunity includes traini

AI Trainee Engineer – £45,000–£75,000 – Job Programme.This is a self-funded programme that leads to employment, fees apply.Complete the programme and get a job, or get your course fees back.Looking to start a career in AI Engineering?.We are offering a structured pathway into AI Engi

Optical Precision is seeking a CNC Turner, Programmer and Setter for a late shift on a four-day week.

We can SolviT Recruitment LTD is seeking an experienced CNC Miller setter/programmer to join a precision sub-con workshop in Shropshire.

TechNichols Resourcing Ltd in the United Kingdom is seeking a Mazak Turning Programmer / Setter/Operator to program, set and operate CNC turning/milling machines, producing precision components to engineering drawings in aerospace and defence sectors.

Ernest Gordon Recruitment is seeking a CNC Programmer for a rapidly growing specialist manufacturing business in Lambeth.

We are seeking a skilled CNC Programmer in Luton, Bedfordshire, offering a £40,000 salary with overtime and long-term career development.

CNC Programmer (Specialist Manufacturing) £55,000 - £65,000 + Rapidly growing company + Equity + Company Bonus + Days Based + Monday to Friday + Progression + Company Benefits Lambeth Are you a CNC Programmer or similar looking for a one of a kind opportunity to join a forward-thinking, fast growt

Morson Edge is seeking a CMM Programmer for its Warton site on a 12-month contract.

Recruit4staff, on behalf of a well-established precision engineering company, is seeking a CNC Turner Programmer/Setter to join their Crewe team.

Wec Group Ltd in the United Kingdom is seeking an experienced CNC Machinist to program, set and operate vertical machining centers in a fast-paced cell.The role requires efficient setups and close involvement in inspection.The ideal candidate has at least five years post-qualification experience in

A newopportunity to join a team working within multiple sectors including Aerospace, Automotive and Oil & Gas as a CNC Milling Programmer. Lead CNC Milling Programmer Responsibilities:. Lead CNC Milling Programmer Experience:.

Roche in the United Kingdom is seeking an Analytical Data Science Programmer to transform statistical analysis plans into high-quality, traceable programming outputs for clinical studies, including TLFs, datasets (SDTM/ADaM), and interactive visualizations.

The Programmer Setter Operator will produce components to drawing tolerances within quality specs and apply machining methods to achieve production targets.

CAM Programmer Location: London SE1 Job Type: Full-time Salary: Competitive DOE Role Overview We are seeking an experienced CAM Programmer to join our growing manufacturing team in Southwark.

In this role, you will be responsible for running and programming punch and laser machinery within a busy engineering environment based in Luton.This is a state-of-the-art facility with sites across Europe, offering excellent opportunities for development and long-term career progression.The company

ViiV Healthcare in Durham seeks an experienced Lead Programmer to drive programming for multiple studies, ensuring efficient analysis package development and validation.

MTrec Ltd Technical is seeking a skilled CNC Turning Programmer/Horizontal Borer Programmer to join our client’s workshop.

AV is seeking an experienced System Programmer to join our Programming team.

Seeking a Project Planner with experience of creating, maintaining and progressing engineering schedules for large scale EPIC projects at Heathrow Airport.They should be able to develop programmes and see them through from project conception to close-out - often interfacing with other projects.The s

Skillsearch is partnering with a leading AAA game developer to find a talented Senior Engine Programmer to join their team. Senior Engine Programmer – AAA Games Studio – Hybrid, UK Games Hub.

Streamline Search are seeking an experienced CNC Miller to join a specialist precision engineering business in the United Kingdom.The role covers programming, setting and operating Mazak milling centres to produce precision components to tight tolerances.You will read and interpret detailed drawings

This is an exciting opportunity for an exceptional, experienced System Programmer to join an established operation with scope to drive and enhance the service at every opportunity. Work alongside other proAV® programmers and as part of the team will be expected to assist your colleagues when requir

IQVIA is seeking an experienced PK/PD Statistical Programmer to support Pharmacometrics with high-quality, NONMEM-ready PK/PD datasets and advanced R programming.

Enterprise Recruitment Ltd is seeking a candidate to run and program punch and laser machinery in a busy engineering environment in Luton.This state-of-the-art facility supports development and long-term career progression.The role requires experience programming punch and laser machines, with a min