You will be instrumental in supporting Health Technology Assessment (HTA) submissions and providing expert statistical advice. Please note that to be considered for this role you must have the right to work in this location.
You will have a BSc (or higher) in Statistics or Mathematics. Previous experience working in a regulated or manufacturing environment, and SAS/R programming are advantageous. We will expect you to be able to successfully contribute to and manag a small number of projects, and work with colleagues from a range of backgrounds to explain statistical concepts to them.
Senior Consultant - Health Economist/Statistician Location - London or Winchester with hybrid working as per departmental requirements (currently a MINIMUM of 40% (2 days per week) with Tuesday as the team day. In LCP launched our Heath Analytics practice, providing analytical and research services for organisations across the life sciences and healthcare industries. Our team brings together...
You will join a large, well-established group of statisticians and will work on trials designed to answer questions of real importance that will contribute to improved care pathways and patient outcomes across a range of long-term health conditions of strategic importance to NHS, patients and social care.
Job Description We are looking for an experienced statistician who has an interest in applied statistical methods for evidence synthesis. We are looking for an enthusiastic and motivated individual who is proactive, shows initiative, and has experience in contributing to the design and execution of statistical analyses, reporting results and mentoring fellow statisticians. The role will be based...
You will be presented with the opportunity to apply techniques learned during your academic training to real-world problems in healthcare and medical science.
You will work on projects involving data analysis and the communication of both methodologies and results in a variety of publications, value materials, health economic models or health technology assessment submissions.
Job Summary This post is an opportunity to join our committed team of statisticians for a year and become involved in extremely rewarding work, developing a broad range of statistical and other skills. The post will involve collaborative work with clinicians and others working in organ transplantation, blood donation and haematology. This post is for undergraduate students studying for a degree...
Research Statistician Developer Intern- Glasgow Summer R&D Internship 2026 Job Locations UK-Glasgow Requisition ID 20067579 Job Category Intern Travel Requirements None Glasgow Summer R&D Internship 2026 Research Statistician Developer Intern - Hybrid Glasgow Summer 2026 Nice to meet you! We’re the leader in analytics. Through our software and services, we inspire customers around the...
You will design and guide statistical strategies across clinical development and post‐approval launch activities.
You will partner with cross‐functional teams including clinical, regulatory, and medical.
You will coach and grow a talented team and help shape how we use data to make better decisions.
We are seeking an Executive Consultant – Vice President of Quantitative Clinical Pharmacology to join our Strategic Consulting team. This role blends scientific leadership, strategic advisory, client relationship development, and technical excellence in population modeling and quantitative clinical pharmacology. The successful candidate will leverage both deep quantitative expertise and strong...
You will need strong prioritisation skills to identify what activities can add the most value and impact, and an ability to upskill others (analysts and non-analysts) and build capability to support the delivery of key pieces of work.
Director Biostatistics | Global Pharma | UK | Home Based | Global Pharma recognised for its commitment to innovation and patient impact, is expanding rapidly in the UK. As part of this growth, the company is offering a rare opportunity for an experienced Director Biostatistics to join them. This is an organisation where excellence is not just expected, it's cultivated. Known for its open,...
You will need strong prioritisation skills to identify what activities can add the most value and impact, and an ability to upskill others (analysts and non-analysts) and build capability to support the delivery of key pieces of work.
You will work on a range of projects involving the set-up and management of de novo, global real-world evidence (RWE) studies, including ethics applications and site support
You will act as the primary contact for study management tasks, providing strategic leadership and ensuring high-quality delivery in line with ethical and regulatory standards.
You will design and guide statistical strategies across clinical development and post‐approval launch activities.
You will partner with cross‐functional teams including clinical, regulatory, and medical.
You will coach and grow a talented team and help shape how we use data to make better decisions.
2 days ago Be among the first 25 applicants Direct message the job poster from Warman O'Brien Principal Biometrics Consultant @ Warman O'Brien Limited | Recruiting Statisticians Join a leading global healthcare organization committed to delivering innovative solutions where patient needs are highest. This organization pioneers scientific advancement in under-served and rare disease areas,...
You will be instrumental in supporting Health Technology Assessment (HTA) submissions and providing expert statistical advice. Please note that to be considered for this role you must have the right to work in this location.
About Us: Join our Medical Devices Centre of Excellence in Witney, where we are at the forefront of developing the next generation of glucose-monitoring technology. With strong business growth and innovative product development, we have an exciting opportunity for a Senior Statistician I to make a significant impact on patient health. The Role: As a Senior Statistician I, you'll be involved in...
You will work on a range of projects involving the set-up and management of de novo, global real-world evidence (RWE) studies, including ethics applications and site support
You will act as the primary contact for study management tasks, providing strategic leadership and ensuring high-quality delivery in line with ethical and regulatory standards.
You will act as the primary contact for study management tasks, providing strategic leadership and ensuring high-quality delivery in line with ethical and regulatory standards.
You will take pride in producing exceptionally high-quality work and will relish the opportunity to build successful relationships with clients, as well as internal colleagues.