10 of 10 Permanent Pharmaceutical Jobs in Uxbridge

governance, compliance, and delivery excellence. Preferred Qualifications SAP Business Data Cloud, SAP Datasphere, SAP Analytics Cloud, or SAP BTP certifications. Experience in Life Sciences, Pharmaceutical, Biotechnology, or highly regulated industries. Experience with Microsoft Fabric, Azure Data Platform, Snowflake, Databricks, or other modern cloud data ecosystems. Strong knowledge of AI-driven ...

Excellent analytical and problem‐solving skills. Working knowledge of IT processes (i.e., ITIL) including incident, problem, defect, change, etc. Prior working experience in a pharmaceutical company is preferred. Excellent presentation, facilitation, and diplomacy skills. Able to perform other duties as assigned. Ability to document technical solutions with excellent organization ...

people around you more effective It'd be a bonus if you also have... Deep experience supporting global regulatory filings (NDA, BLA, MAA) within pharma clinical development Broad knowledge of the end‐to‐end drug development process and global regulatory frameworks Experience with R or other statistical programming languages Familiarity ...

offering a wide range of products for both standard and specialist industrial applications. They supply to all market sectors including oil/gas, chemical, pharmaceutical, medical, food, motor racing, semiconductor and power generation. The Role The Applications Engineer will be responsible for preparing technical proposals, taking company products through ...

culture here that wants to hear them. You’ll thrive here if you... Have 7+ years of statistical programming experience in the pharmaceutical or biopharma industry, including hands-on involvement in major regulatory submissions Are deeply fluent in SAS, CDISC/SDTM/ADaM standards ...

office time in Uxbridge, with collaboration across Biostatistics, Data Science, HEOR, Epidemiology, Clinical, and IT teams. Ideal candidates have 3+ years in RWE with pharma/clinical trials, strong SAS/R/Python skills, and ability to communicate complex concepts to non-technical stakeholders. #J-18808-Ljbffr ...

clinical data into submission-ready outputs for regulators, using SAS and CDISC standards to shape regulatory submissions and patient outcomes. With 7+ years in pharma statistical programming, you will influence strategy, mentor others, and lead electronic #J-18808-Ljbffr ...

related field.* 3+ years of experience working with real-world healthcare data (claims, EMR, registries, etc.).* 2+ years of experience in pharmaceutical industry (e.g. Pharma, CRO, Biotech) and clinical trials.* Proficiency in SAS, R, Python, or similar tools for data manipulation and analysis. AI/ML knowledge ...

Regeneron Pharmaceuticals, Inc. is seeking an Associate Director to lead companion diagnostic (CDx) strategy, bridging translational science with diagnostic execution. You will own CDx programs from feasibility through clinical validation and regulatory submission to launch ...

Bristol Myers Squibb is seeking an experienced RWE Analyst to curate, transform, and analyze real-world data to inform evidence generation and trial design. This on-site role requires 50% office time in Uxbridge and ...