We are looking for a Senior Quality Inspector to join our Christchurch, Dorset team! As a Senior Quality Inspector, working within a small quality team, you will be undertaking the quality inspection of manufactured goods ensuring
Clinical trials are high stakes, demanding high standards. Veramed sets this standard by bringing together the sharpest minds in data management, biostatistics and programming, with cutting-edge technology and proven processes. Our globally connected, caring team delivers
We are currently supporting a biometric specialist organisation with a large scale build out of their FSP statistics team across the UK, Spain and France. My client is looking for multiple Senior and Principal Biostatisticians to
Principal Project Lead Biostatistician – Leading CRO – Homebased – UK / Europe We have recently partnered with an award winning CRO, who are looking for an experienced Principal Statistician to join their successful study delivery
Senior Statistician | UK | Remote | Mid-Size CRO | Permanent Our client is an established specialist biometrics consultancy providing high-quality statistical and programming services to the pharmaceutical and biotechnology industry. Due to continued growth, they are
The Principal Biostatistician will serve as study statistician or support statistician on Bronchiectasis or Hepatitis B programs. TA experience is an advantage but not essential. Primary Responsibilities: Responsible for protocol development including study design, sample size
Senior Director, Global Biometrics | Global Pharma| Hybrid | UK / France | Permanent An exciting opportunity has arisen for an experienced Senior Director, Biometrics to join a global, innovation-led pharmaceutical company at a pivotal stage
Freelance Statistician | Indirect Treatment Comparisons | Network Meta Analysis | HTA | UK Based | Outside IR35 | £35-£45 Per/Hour | 40 hours per week | 6 month contract | ASAP Start We are partnering with
Contract Statistician We are seeking an experienced Contract Statistician to support clinical development from early to late-stage development. The successful candidate will need to have extensive experience in the statistical design, analysis, and reporting of clinical trials across