Senior Statistical Programmer – FSP | Global CRO | Fully Remote | UK | Europe | A globally recognized CRO, is seeking an experienced Senior Statistical Programmer to join their FSP team. In this role, you will lead programming activities for complex clinical studies, manage resources, allocate tasks, and track progress to meet project timelines and quality standards. Key Responsibilities: Lead programming for multiple complex studies. Develop datasets, tables, figures,...
Senior Statistical Programmer - Join a World-Leading CRO UK | Ireland | Poland | Hungary | Romania | Bulgaria | Slovakia | Slovenia | Spain | Join a globally renowned CRO that is expanding its Statistical Programming team across the UK and Europe. This innovative organisation is driven by excellence and firmly believes in investing in its people, recognizing them as its greatest strength and the driving force behind its...
Clinical Programmer – FSP | Global Leading CRO | UK | Home Based | A leading global CRO is hiring a Clinical Programmer to join their team. You’ll be fully integrated into a dedicated sponsor that values performance, recognizes merit, and prioritizes quality. This supportive environment encourages innovation, individuality, and teamwork. The role is fully remote. What you will be doing: Collaborate with Data Managers and Clinical Standards teams to...
Senior Statistical Programmer – FSP | Leading CRO | UK | Europe | Fully Remote | Permanent | A leading global CRO, recently recognized as Best Employer, is seeking a Senior Statistical Programmer to join their FSP team. This fully remote role is available to candidates based in the UK or Europe. Key Responsibilities: Lead multiple studies predominantly Phase II-III Develop datasets, tables, figures, and listings Requirements: Degree in computer...
Associate Director / Head of Biostatistics - Top Pharma - UK / Belgium / Netherlands / France Our client, a leading global pharma is looking for an expert biostatistician to join, their dynamic team, working on exciting projects in Rare disease. You will require Line Management experience, as well as regulatory interactions. Purpose Provide statistical expertise and contributions for projects and protocols in support of Drug Development Programs Provide statistical...
Senior Bioinformatician Who are they? I’m working with a stealth mode organisation who are an Oxford University spin off early-stage genetic therapy platform company. They’re advancing precision medicine by harnessing the power of protein isoforms, specifically focusing on treating neuromuscular diseases of high unmet needs. This company is backed by an established venture capital investor and have a clear mission to improve lives through genetic medicine. Key responsibilities: Collaborating closely...
Associate Director of Biometrics We are partnered with a clinical stage Pharma company who are dedicated in advancing next generation targeted radiopharmaceuticals to treat cancer patients. The AD of Biometrics will act as the lead statistician on clinical studies as part of the wider project team. To be successful in this role you will have the ability to work in a fast paced team environment, prioritizing your work across multiple...
Head of Medical Writing and Regulatory Affairs The Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This is a hybrid role in Central London. Applicants must be prepared to go on site 4 days per...
Technical Writer – Quality Assurance (UK – Remote) Warman O’Brien proud to be partnered with a leading Consulting Firm looking for Technical Writers on behalf of a leading Mid-Size Biotechnology Company. As a part of a global transformation project we’re looking for a team of Technical Writers to support this Biotech’s Quality teams (SMEs) to develop SOPs, quality documents and procedures for the department. If you have the below experience...
We are seeking a highly skilled and motivated Commercial Qualified Person (QP) to join our client, a well-established global pharmaceutical organisation. As a Commercial QP, you will play a critical role in ensuring compliance with regulatory and quality standards for commercial activities related to the distribution, sale, and marketing of pharmaceutical products. Your primary responsibility will be to oversee the release of products for commercial distribution and ensure their continued...
Senior Biostatistician United Kingdom (remote) Start Date: ASAP Up to £80k A globally recognized CRO is seeking a Senior Biostatistician to contribute to ground-breaking projects in the pharmaceutical, biotechnology, and medical device sectors. What will you be doing? Oversee statistical and programming tasks, ensuring accuracy, efficiency, and timely project delivery. Design, analyse, and report clinical trials with precision; write Statistical Analysis Plans (SAPs) and ensure quality results. Develop and validate...
Principal Biostatistician United Kingdom (remote) Start Date: ASAP Up to £90k Join a global CRO recognized for its excellence in statistical analysis and data management. This client is seeking a Principal Biostatistician to lead clinical programs, mentor teams, and deliver high-impact results for ground-breaking therapies. What will you be doing? Manage clinical trial programs, provide operational oversight, and ensure sound statistical methodologies. Coach and guide biostatisticians and statistical programmers, fostering...
Principal Lead Statistical Programmer | Pharma | UK | Netherlands | Italy | France | Home Based Expanding globally this European Pharma who are focussing on developing and commercializing innovative prescription drugs, particularly in the areas of respiratory, neonatology, rare diseases, and specialty care, are looking for an experienced Principal Statistical Programmer to join them. This is an exciting opportunity for an experienced and ambitious Statistical Programmer, who is looking...
Niche Opportunity Associate Director of Biometrics - Innovative Biopharma - Oncology - UK I am currently looking for a talented and motivated Associate Director of Biometrics to join an exciting Pharma company based in Oxford. This gives you the opportunity to work as the sole statistician, within a growing team and is offered remote / hybrid. Principal Statisticians also considered if you are looking for your next step in your...
A Global CRO have partnered with a leading Pharma company and they require a Contract Principal Statistician. This contract role will involve working within Respiratory Therapeutic Area. Details: Respiratory Early Phase, phases I and II Complex studies, need to communicate effectively internally and with customer Work with Global Pharma company Inside IR35 Umbrella They offer: Interviews Starting ASAP Full Time Contract Hourly Rate: £62ph Flexible Working Hours Remote (Homebased) Great...
Join a company at the forefront of healthcare innovation Specializing in cutting-edge monitoring systems for home and hospital use, this organization is passionate about enhancing lives through ground-breaking technology. With the launch of their latest system, they are looking for a talented Senior Statistical Programmer to be part of their journey. Step into a dynamic R&D environment where innovation drives everything. This role offers the chance to contribute to life-changing...
Niche Opportunity Associate Director of Biometrics - Innovative Biopharma - Oncology - UK I am currently looking for a talented and motivated Associate Director of Biometrics to join an exciting Pharma company based in Oxford. This gives you the opportunity to work as the sole statistician, within a growing team and is offered remote / hybrid. Principal Statisticians also considered if you are looking for your next step in your...
Head of Medical Writing and Regulatory Affairs The Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This is a hybrid role in Central London. Applicants must be prepared to go on site 4 days per...
Senior Statistical Programmer – FSP | Global CRO | Fully Remote | UK | Europe | A globally recognized CRO, is seeking an experienced Senior Statistical Programmer to join their FSP team. In this role, you will lead programming activities for complex clinical studies, manage resources, allocate tasks, and track progress to meet project timelines and quality standards. Key Responsibilities: Lead programming for multiple complex studies. Develop datasets, tables, figures,...
Join a company at the forefront of healthcare innovation Specializing in cutting-edge monitoring systems for home and hospital use, this organization is passionate about enhancing lives through ground-breaking technology. With the launch of their latest system, they are looking for a talented Senior Statistical Programmer to be part of their journey. Step into a dynamic R&D environment where innovation drives everything. This role offers the chance to contribute to life-changing...
Senior Statistical Programmer - Join a World-Leading CRO UK | Poland | Romania | Bulgaria | Slovakia | Slovenia | Hungary | Join a globally renowned CRO that is expanding its Statistical Programming team across the UK and Europe. This innovative organisation is driven by excellence and firmly believes in investing in its people, recognizing them as its greatest strength and the driving force behind its success. As a Senior...
Clinical Programmer – FSP | Global Leading CRO | UK | Home Based | A leading global CRO is hiring a Clinical Programmer to join their team. You’ll be fully integrated into a dedicated sponsor that values performance, recognizes merit, and prioritizes quality. This supportive environment encourages innovation, individuality, and teamwork. The role is fully remote. What you will be doing: Collaborate with Data Managers and Clinical Standards teams to...
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