1 to 25 of 31 Biostatistics Jobs in London

computational oncology, machine learning, and data science methodologies. Manage multiple projects simultaneously and ensure timely, high-quality deliverables. Must-Haves: MSc/PhD in data science, computational biology, bioinformatics, biostatistics, or a related field. 3+ years of professional experience in biotech, pharma, or academia focusing on life science projects (ideally oncology drug discovery). Strong foundation in statistics, data analysis More ❯

client relationships, and ensuring optimal project delivery in line with organizational goals. Strong leadership and people management capabilities are a must. With a Master’s degree (or equivalent) in Biostatistics, Data Science, Life Sciences, Business Administration, or a related field and 12+ years of progressive leadership experience in biostatistics, clinical research, or related life sciences consulting organizations. Key responsibilities: P … requirements. Talent Development: Foster a culture of excellence, collaboration, and professional growth. Oversee talent management strategies, including recruitment, retention, and succession planning. Education : Master’s degree (or equivalent) in Biostatistics, Data Science, Life Sciences, Business Administration, or a related field. Experience : 12+ years of progressive leadership experience in biostatistics, clinical research, or related life sciences consulting organizations. Proven experience with More ❯

collaborate closely with global partners in academia, healthcare, and industry to drive innovation and maximise translational impact. The post holder is required to hold a PhD degree in statistics, biostatistics, epidemiology, health data science, or other closely related disciplines. They will bring internationally recognised expertise in statistics and methodological leadership in digital trials, demonstrated by a strong record of publications …/08/2029. About You To be successful in this role, we are looking for candidates to have the following skills and experience: Essential criteria PhD in statistics, biostatistics, epidemiology, health data science, or other closely related disciplines. Proven internationally recognised leadership in the development and implementation of innovative statistical and methodological approaches, particularly in design and conduct of More ❯

software tools (such as WinBugs, R, Stata, Python, and SAS) to drive project success. This role requires a Master's or Doctoral Degree in Health Economics, Health Policy, Statistics, Biostatistics, Mathematics, or other related quantitative fields. Knowledge And Experience Training and extensive experience in health economics, including the conceptualization and development of systematic literature reviews and network meta-analyses (8+ More ❯

define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯

including mentoring/coaching junior members of the team, manage and collaborate with an extended global team of diverse skill sets. What You’ll Bring Demonstrated advanced expertise in biostatistics and/or bioinformatics applications, such as epidemiology, population genetics, genomics, proteomics, bulk or single cell RNA-sequencing, and/or systems biology. Demonstrated leadership the use of in silico More ❯

Location: London Reporting to: Executive Director Biostatistics The Senior Statistical Programmer at Orchard Therapeutics is a key member of a Biostatistics team working to provide transformative gene therapies to patients. Reporting to the Executive Director Biostatistics, this role provides a unique opportunity to use your programming skills in the production of data analyses from all phases of clinical drug development. … Required Knowledge · 3+ years of experience in clinical trial SAS programming. · Demonstrated knowledge of and experience in applying CDISC standards. · Self-starter with the ability to work within a Biostatistics team. Skills and Abilities · Proficiency with SAS programming and SAS macro code development required along with a good understanding of SAS GRAPH and SAS ODS. · Understanding of clinical trial data More ❯

in need of qualified and focused driven individuals for SAS Programmer role to be office-based in London UK. This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming background. At Medpace, our SAS Programmers go through an extensive onboarding and training process, which prepares them to become More ❯

several studies, a medium to large sized project or project-level activities (incl. submission and post-marketing activities). The position is a key collaborator and strategic partner with biostatistics in ensuring that pharmaceutical drug-development plans in Novartis Global Drug Development are executed efficiently with timely and high-quality deliverables. This role offers hybrid working, requiring 3 days per More ❯

culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. ICON’s Global Biostatistics & Statistical Programming team continues to grow and we are looking for experienced Programmers to join this diverse and growing group. Our team is currently over 600 employees in 30+ countries More ❯

Series B round from Balderton Capital, with support from Creandum, Firstminute, Seedcamp, and Visionaries. About the role Lindus Health are looking for a Statistical Programmer to join our Clinical Biostatistics team. This is a pivotal role in scaling our clinical data capabilities, ensuring efficient and high-quality clinical trial data processing and analysis. We’re looking for someone with experience … of statistical programming in R, clinical trial data standards, and regulatory requirements to support high-quality, efficient, and reproducible analyses. You will work closely with our Associate Director of Biostatistics and Data Management, Associate Director of Clinical Data Innovation, biostatisticians, and data managers to enhance data workflows, automate processes, and support clinical trial reporting. About you Degree and/or … library of R functions for common clinical trial analyses Support biostatisticians by creating reusable code for standard analyses (e.g., AE tables, demographic tables) Review SAPs in collaboration with the Biostatistics team and troubleshooting early before implementation Documentation & Knowledge Management Help us to create a foundation for consistent quality across projects and faster onboarding of new team members Document code and More ❯

running pipelines in Nextflow. Ability to communicate effectively with stakeholders from diverse backgrounds and understand clinical and phenotypic data management issues. Qualifications A PhD in Statistical or Computational Genetics, Biostatistics, Population Genetics, or a related quantitative discipline. Additional Information Salary from £55,000. We offer comprehensive benefits, including generous leave, flexible working arrangements, pension schemes, learning and development support, recognition More ❯

and adapt accordingly the AI solutions. Cross-functions high adaptability to meet cross organization goals. Required/Preferred Education Advanced degree (MS or PhD) in Data Science, Computer Science, Biostatistics, or related field 3 - 5 years of related professional experience, with 1+ years of experience applying AI/ML techniques to healthcare or clinical research data. Experience in healthcare/ More ❯

This job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board. The Role This role is responsible for designing, implementing, managing, and optimising our IT infrastructure. This role requires a deep More ❯

View more categories View less categories Discipline Data Management/Statistics ,Biostatistics Hours Full Time Contract Type Permanent Experience Level Experienced (non-manager) The ICOA (Integrated Clinical & Operational Analytics) service contributes to developing the Reporting & Metrics strategy aligned with BI services, optimizing platform usage across GD and Cross Sector. You will maintain and optimize reporting and metrics platforms, ensuring they More ❯

cloud-based platforms and services, in particular AWS. Familiarity with code version control and MLOps deployment approaches. Minimum Requirements Advanced degree (MS or PhD) in Data Science, Computer Science, Biostatistics, or related field 3 – 5 years of related professional experience, with 1+ years of experience applying AI/ML techniques to healthcare or clinical research data. Experience in healthcare/ More ❯

the Medical Monitors to support cross functional departmental communication as applicable on data capture/review trends (e.g., Medical Monitoring, Safety, Clinical Operations, Project Management, Data Management, SAS Programming, Biostatistics, Translational Science, other vendors, etc.) to meet project deliverables in compliance with GCP/ICH, the protocol, oncology standards and applicable Project Plans and SOPs Provides input into project related More ❯

inform internal teams and external stakeholders. Lead simultaneous client facing projects across ZS Discovery to reinvent pharmaceutical discovery, elucidate complex disease biology and pioneer novel therapeutics. Provide expertise in biostatistics and/or bioinformatics applications, such as epidemiology, population genetics, genomics, proteomics, bulk or single cell RNA-sequencing, and/or systems biology. Partner with ZS leaders and client service More ❯

computational oncology, machine learning, and data science methodologies. Manage multiple projects simultaneously and ensure timely, high-quality deliverables. Must-Haves: MSc/PhD in data science, computational biology, bioinformatics, biostatistics, or a related field. 3+ years of professional experience in biotech, pharma, or academia focusing on life science projects (ideally oncology drug discovery). Strong foundation in statistics, data analysis More ❯

regulatory policies. Perform hands-on analysis of integrated clinical trial and real-world data to generate evidence for decision-making in drug development. Your Experience Ph.D. in data science, biostatistics, or a related quantitative field (or equivalent). Over 6 years of experience in clinical drug development with extensive clinical trial exposure. Strong knowledge of statistical methods like time-to More ❯

adapt accordingly to the AI solutions. Cross-functions high adaptability to meet cross organization goals. Required/Preferred Education Advanced degree (MS or PhD) in Data Science, Computer Science, Biostatistics, or related field 7 – 10 years of related professional experience, with 3+ years of experience applying AI/ML techniques to healthcare or clinical research data. Experience in healthcare/ More ❯

Join to apply for the Principal Biomarker Biostatistician role at TREIZE-QUARANTE (1340) 1 day ago Be among the first 25 applicants Join to apply for the Principal Biomarker Biostatistician role at TREIZE-QUARANTE (1340) Get AI-powered advice on More ❯

and adapt accordingly the AI solutions. Cross-functions high adaptability to meet cross organization goals. Required/Preferred Education Advanced degree (MS or PhD) in Data Science, Computer Science, Biostatistics, or related field 3 - 5 years of related professional experience, with 1+ years of experience applying AI/ML techniques to healthcare or clinical research data. Experience in healthcare/ More ❯

and adapt accordingly the AI solutions. Cross-functions high adaptability to meet cross organization goals. Required/Preferred Education Advanced degree (MS or PhD) in Data Science, Computer Science, Biostatistics, or related field 3 – 5 years of related professional experience, with 1+ years of experience applying AI/ML techniques to healthcare or clinical research data. Experience in healthcare/ More ❯

awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/ More ❯