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...

Pfizer is seeking a statistics expert to design, analyze, and interpret clinical trials and observational studies in line with regulatory requirements and Pfizer standards. You will provide scientifically rigorous...

We make health happen At Bupa, our purpose is helping people live longer, healthier, happier lives and making a better world. As a healthcare provider and insurer, we support millions of people through every stage of...

YOU MAKE US MORE Join Moorfields Eye Hospital NHS Foundation Trust At Moorfields, people’s sight matters—and so do the people who make it possible. For over 200 years, Moorfields has been at the forefront of...

Job summary We are seeking applicants for a full-time substantive (8PA) post in Paediatric Endocrinology at Alder Hey Children's Hospital. The successful applicant will be expected to support general endocrinology and...

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.