Harvey Nash Group in Welwyn Garden City, UK is seeking a Senior Data Manager to lead data management activities across clinical studies, including CRF design, data cleaning, and vendor oversight. The role emphasizes...

Employer Cumbria, Northumberland, Tyne and Wear NHS Foundation Trust Employer type NHS Site West Farm House Town Cramlington Salary £104,401 - £115,341 pro rata for part time Salary period Yearly Closing 09/11/ :59...

Bristol Myers Squibb in Uxbridge is seeking an Associate Director of Biostatistics to join cross-functional development teams. You will contribute to trial design, analysis planning, and regulatory submissions, with...

Johnson & Johnson in Buckinghamshire, United Kingdom, seeks a Senior Statistical Programming Lead to plan, oversee and deliver statistical programming activities across one or more clinical projects. You will guide...

The Role Veeva's Vault Clinical Data Management System (CDMS) is changing how life sciences companies manage clinical trial data, bringing EDC, coding, and Data Quality System (DQS) together in one platform. The...

Job overview We are recruiting for a full-time Consultant Psychiatrist to join Melksham Community CAMHS and work with a well-established multi-disciplinary team at Melksham Community Hospital in Wiltshire. You'll...

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely as part of a sponsor-dedicated team. You will implement reporting and analysis activities for sponsor trials, oversee CRO...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed...

Cytel Inc. is seeking a Senior/Principal Statistical Programmer to join a sponsor-dedicated program, embedded with a pharmaceutical client. You will independently manage programming deliverables across SDTM/ADaM,...

Principal Statistical Programmer needed for pharmaceutical client to develop SAS/R programs for clinical trials, manage CROs, and support regulatory submissions.