slough, south east england, united kingdom Hybrid / WFH Options
IXICO
the role: Essential Bachelor’s degree in Computer Science, Life Sciences or related field preferred, or equivalent experience required. 1+ years’ experience of working in data management within the Pharmaceutical, Biotech or CRO industry recommended. Strong IT skills (working within cloud-based database systems desirable) and demonstrate experience of working with a variety of data formats. Experience working with Microsoft More ❯
slough, south east england, united kingdom Hybrid / WFH Options
Vallum Associates
you will bring domain and technology expertise to help shape and drive a set of innovative, transformational work across different industry market sectors (Utilities, Retail, CPG, Energy, Telecom, BFSI, Pharmaceutical & Lifesciences and Government). Job Responsibilities: • Take responsibility for steering Celonis projects and programs aimed at enhancing operational performance, ensuring future-ready operations, and developing sustainable AI-led capabilities within More ❯
Reading, Berkshire, United Kingdom Hybrid / WFH Options
IQVIA LLC
you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work on a team where your role is both challenging and rewarding, while working alongside colleagues who are passionate about influencing … dedicated to reshaping the future of healthcare. Additional Benefits: Home-based remote work opportunities Great work/life balance Collaborate on projects and innovations with industry leaders in the Pharma and CRO sectors Cohesive team environment fostering a collaborative approach to study work Variety of therapeutic areas, indications and, study phases Job stability; long-term engagements and development opportunities Career … Science, Mathematics, Statistics or related area with relevant experience Experience • At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software. • Indepth understanding of clinical programming and/or statistical programming processes and standards. • Indepth understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH). More ❯