Job Overview: As a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs, across complex projects and studies. This involves planning and coordinating
The Senior Statistical Programmer will be responsible for review datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs
Lead and execute clinical and operation advanced analytics or system improvements Develop novel data science methodologies to generate deep insights from disparate data sources. Provide subject matter expertise to teams in identification and application of the
Job Summary: This position is responsible for the development of the end to end design of client standards and study specifications that align to the CDISC standards and regulatory agency guidance’s. This position provides this guidance
Senior Statistical Programmer I / II | Leading CRO | Home Based | UK | Permanent | Join a fast-growing, independent CRO providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical
Greetings! Tech Observer, a Global Clinical Research Organization (CRO) & FSP provider that has been supporting the Pharmaceuticals & Life Sciences Industry since 2005. We have offices in New Jersey, US (Headquarters), India, Denmark, UK &
Freelance HEOR Consultant | HTA Statistician | Evidence Synthesis | UK & Europe | 6 Months Contract | Remote | Flexible FTE | ASAP Start We are partnering with a leading global life sciences consultancy that
HTA Statistician Health Economics | HTA | Evidence Synthesis | Market Access We are supporting a growing team looking for an HTA Statistician to deliver high-quality statistical and evidence synthesis projects for global pharmaceutical and biotech clients.
Director – Biostatistics (Asset Lead)- Oncology – Pharma – UK – Remote / Hybrid We are seeking an experienced and highly skilled Biostatistics Director to join a cross-functional team in a leading global pharmaceutical environment. This
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
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
Senior Director, Global Biostatistics | Global Pharma| Hybrid | UK / France | Permanent An exciting opportunity has arisen for an experienced Senior Director, Biostatistics to join a global, innovation-led pharmaceutical company at a pivotal stage
Biomarker Lead Statistician ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to
Overview IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. IQVIA has two teams focused exclusively on amplifying the patients voice and enhancing their experiences across