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Senior Clinical Statistical Programmer (Portfolio Development / Biometrics / Programming) The Role CSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package. 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 hold up under regulatory scrutiny, and the person who decides how a dataset gets built, not just who builds it. You'll work alongside statisticians, data managers, medical writers and regulatory colleagues as a peer, not a downstream resource — reading protocols and SAPs early enough to shape how a study's analysis gets structured, then seeing that structure through to submission-ready SDTM and ADaM datasets, TFLs, and supporting documentation. Hybrid Based (3 days a week onsite) in Maidenhead Why It Matters Clinical data is only as useful as the programming behind it is trustworthy. Every regulatory decision downstream — every safety signal caught or missed, every submission accepted or queried — traces back to whether the datasets and outputs were built right the first time. This role sits at that pressure point. You're not just executing specifications; you're often the one writing them, catching the ambiguity in a protocol before it becomes a data problem three months later, and making the judgment calls that keep a study's analysis both scientifically sound and audit-ready. What You'll Be Responsible For You'll lead end-to-end programming for your assigned studies — in-house or outsourced — spanning the full clinical development lifecycle from study setup through analysis, reporting, and regulatory submission. That means building and validating datasets and outputs yourself where the work is done internally, and holding CRO-delivered work to the same bar where it isn't. You'll also be a technical reference point for less experienced programmers, and a contributor to how the wider programming function does its work. · Serve as lead programmer for one or two clinical trials, interpreting protocols, SAPs, data management plans, and CRF specifications to drive study setup and analysis · Design and validate SDTM and ADaM datasets, tables, figures, and listings, in partnership with study statisticians · Review and take ownership of CRO-produced deliverables, ensuring submission-ready quality before they go further · Lead specification and delivery of integrated analyses (e.g. ISS/ISE) and associated outputs when not handled by a CRO · Mentor other programmers on internal processes and standards, and contribute to departmental tools and process improvements · Take on ad hoc analytical work — regulatory query responses, exploratory analyses, publication support — as studies require it Experience Required · Experience of programming in pharmaceutical, biotech, CRO, or clinical research settings · Strong SAS proficiency (Base/Macro/Stat/Graph); familiarity with R or other languages is a plus · Working knowledge of current CDISC standards — CDASH, SDTM, ADaM, define.xml · Track record of producing and validating submission-ready TFLs and datasets, including ad hoc analytical requests · Experience supporting regulatory submissions (FDA required; PMDA, NMPA, or EMA experience a plus) · Comfort working with external vendors and CRO-managed data · BSc in Computer Science, Mathematics, Statistics or a related field — equivalent experience and certifications will also be considered

Senior Clinical Statistical Programmer (Portfolio Development / Biometrics / Programming)The RoleCSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package. 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 hold up under regulatory scrutiny, and the person who decides how a dataset gets built, not just who builds it. You'll work alongside statisticians, data managers, medical writers and regulatory colleagues as a peer, not a downstream resource — reading protocols and SAPs early enough to shape how a study's analysis gets structured, then seeing that structure through to submission-ready SDTM and ADaM datasets, TFLs, and supporting documentation.Hybrid Based (3 days a week onsite) in MaidenheadWhy It MattersClinical data is only as useful as the programming behind it is trustworthy. Every regulatory decision downstream — every safety signal caught or missed, every submission accepted or queried — traces back to whether the datasets and outputs were built right the first time. This role sits at that pressure point. You're not just executing specifications; you're often the one writing them, catching the ambiguity in a protocol before it becomes a data problem three months later, and making the judgment calls that keep a study's analysis both scientifically sound and audit-ready.What You'll Be Responsible ForYou'll lead end-to-end programming for your assigned studies — in-house or outsourced — spanning the full clinical development lifecycle from study setup through analysis, reporting, and regulatory submission. That means building and validating datasets and outputs yourself where the work is done internally, and holding CRO-delivered work to the same bar where it isn't. You'll also be a technical reference point for less experienced programmers, and a contributor to how the wider programming function does its work.· Serve as lead programmer for one or two clinical trials, interpreting protocols, SAPs, data management plans, and CRF specifications to drive study setup and analysis· Design and validate SDTM and ADaM datasets, tables, figures, and listings, in partnership with study statisticians· Review and take ownership of CRO-produced deliverables, ensuring submission-ready quality before they go further· Lead specification and delivery of integrated analyses (e.g. ISS/ISE) and associated outputs when not handled by a CRO· Mentor other programmers on internal processes and standards, and contribute to departmental tools and process improvements· Take on ad hoc analytical work — regulatory query responses, exploratory analyses, publication support — as studies require itExperience Required· Experience of programming in pharmaceutical, biotech, CRO, or clinical research settings· Strong SAS proficiency (Base/Macro/Stat/Graph); familiarity with R or other languages is a plus· Working knowledge of current CDISC standards — CDASH, SDTM, ADaM, define.xml· Track record of producing and validating submission-ready TFLs and datasets, including ad hoc analytical requests· Experience supporting regulatory submissions (FDA required; PMDA, NMPA, or EMA experience a plus)· Comfort working with external vendors and CRO-managed data· BSc in Computer Science, Mathematics, Statistics or a related field — equivalent experience and certifications will also be consideredTPBN1_UKTJ

Join Our Team as a Senior Clinical Statistical Programmer!\n The Role \n Are you ready to take the reins of clinical trials from the very first line of code to the final submission package? At CSL, we’re on the lookout for a Senior Programmer who will play a pivotal role in ensuring the integrity and reliability of our clinical data. This is not just any programming position; you’ll be the go-to expert for study teams, ensuring that our datasets withstand regulatory scrutiny and are built with precision. \n Location: Hybrid (3 days a week onsite) in Maidenhead Why It Matters\n In the world of clinical research, the quality of our data is only as strong as the programming behind it. Every regulatory decision—whether it’s a safety signal caught or a submission accepted—hinges on the robustness of our datasets. In this role, you’ll be at the heart of it all, not just executing specifications but also crafting them. Your insights will help catch ambiguities before they escalate into data issues, ensuring that our analyses are scientifically sound and audit-ready. Your Responsibilities\n As the lead programmer for your assigned studies, you’ll oversee the entire clinical development lifecycle, from study setup to regulatory submission. Here’s what you’ll be doing: \n\n • Lead programming efforts for one or two clinical trials, interpreting protocols, SAPs, and data management plans 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 ensure the quality of CRO-produced deliverables, making sure they are submission-ready.\n, • Lead the specification and delivery of integrated analyses (e.g., ISS/ISE) and associated outputs when not managed by a CRO.\n, • Mentor junior programmers on internal processes and contribute to departmental tools and process improvements.\n, • Engage in ad hoc analytical work, including regulatory query responses and publication support as needed.\nWhat We’re Looking For\n To thrive in this role, you should bring the following experience and skills: \n\n • Proven 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, • Working knowledge of current CDISC standards (CDASH, SDTM, ADaM, define.xml).\n, • A track record of producing and validating submission-ready TFLs and datasets, including handling ad hoc analytical requests.\n, • Experience supporting regulatory submissions (FDA experience required; PMDA, NMPA, or EMA experience is a bonus).\n, • Comfort in collaborating with external vendors and managing CRO data.\n, • A BSc in Computer Science, Mathematics, Statistics, or a related field; equivalent experience and certifications will also be considered.\nWhy Join Us?\n At CSL, you’ll be part of a dynamic team that values innovation, collaboration, and professional growth. We offer a supportive environment where your contributions make a real impact. If you’re ready to elevate your career and help shape the future of clinical research, we want to hear from you!

Expert-level command of low-level profiling and debugging suites. Mentor and upskill the engineering team in modern API paradigms and low-level hardware debugging techniques. We’re looking for a Principal Low-Level Graphics Programmer to join our award winning team in Middlesbrough (UK), home to t

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Ensures high quality is built into own deliverables and the quality delivered by other programmers. Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader. Senior Statistical Programmer Consultant.

Senior Statistical Programmer Consultant. Senior Statistical Programmer Consultant.

CNC Miller (Programmer / Setter / Operator).Aerospace Manufacturing | Up to £46800 DOE + Overtime.Monday – Thursday 08:00 – 17:00 (30 minutes lunch break).Friday 08:00 – 13:00 (no lunch break).We're seeking a skilled CNC professional to join a busy aerospace manufacturing environment, produci

CSL is seeking a Senior Clinical Statistical Programmer to own one or two trials from first line code to submission packaging. You’ll shape study analysis, write protocols, and ensure audit-ready datasets and TFLs for regulatory submissions. You’ll lead end-to-end programming, mentor other programmers, and collaborate with statisticians, data managers, and regulatory teams in a hybrid Maidenhead setting. #J-18808-Ljbffr

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CSL is seeking a Senior Clinical Statistical Programmer to take technical ownership of one or two trials from first line of code to submission package.

Senior Clinical Statistical Programmer to own the programming for one or two trials from setup to submission, collaborating with statisticians, data managers and regulatory colleagues.

Gattaca is seeking an experienced CAM Programmer to join our Southwark-based manufacturing team.

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. We are seeking a passi

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 hold up under regulatory scrutiny, and the person who dec

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 hold up under regulatory scrutiny, and the person who decides how a dataset gets built, not just who builds it. Hybrid Based (3 days a week onsite) in

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Senior Clinical Statistical Programmer (Portfolio Development / Biometrics / Programming).

Senior Clinical Statistical Programmer responsible for end-to-end programming of clinical trials, ensuring data integrity and submission readiness.