Profil ist ein 1999 gegründetes, international tätiges und renommiertes Auftragsforschungsinstitut im Bereich der Stoffwechselerkrankungen. Wir arbeiten seit vielen Jahren gemeinsam mit der Pharmaindustrie an der Entwicklung neuer Arzneimittel für die Behandlung von Diabetes, Adipositas und damit
Clinical Data Standards Consultant - ADaMICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion
Make your mark for patientsWe are looking for a Senior Principal Programmer (Statistical Computing Environment Business Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization and Reporting team, based in any of our
Frankfurt, Hesse, Germany Paris, France Barcelona, Spain Paris, France Budapest, Hungary Turku, Finland Dublin, Ireland Athens, Greece Madrid, Spain Copenhagen, Denmark Stockholm, Sweden Full time R + We are seeking an experienced PK/PD Statistical Programmer with
Clinical Data Standards Consultant - ADaM 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
Reading, Berkshire, United Kingdom Belgrade, Serbia Rome, Roma, Italy Paris, France Vienna, Austria Budapest, Hungary Amsterdam, Netherlands Dublin, Ireland Sofia, Bulgaria Frankfurt, Hesse, Germany Athens, Greece Ljubljana - Dunajska, Slovenia Madrid, Spain Brussels, Brussels-Capital Region, Belgium
Senior Statistical Programmer - RICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Pharmacometrics Support ProgrammerICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the
Overview In this role you will support pharmacometrics by creating and QC’ing NONMEM PK/PD datasets, enabling robust modelling across a global clinical portfolio. You will work with Data Management, Statistical Programming, and Bioanalytical teams to ensure
Overview As Director of Biostatistics, you lead statistical input across clinical study teams and programs, owning statistical deliverables and regulatory inputs. You will serve as a biostatistics lead on cross-functional teams, shaping clinical development plans, protocols,
Overview In this role you will drive CDISC-based data standards within a global clinical operations context. You will support operational staff on ADaM and define.xml capture, build tools to improve data delivery quality, and contribute to
Overview In this role you enable clinical programming teams to operate within UCB’s modern Statistical Computing Environment, translating reporting needs into well-governed study setups. You will support compliant platform operations and improve how trial analyses and
Overview As a Senior Statistical Programmer at ICON, you will develop and validate R programs for statistical analysis of clinical trial data, and lead programming teams to produce CDISC-compliant outputs. You will collaborate with biostatisticians to
En ALTEN sabemos que el éxito de nuestros proyectos se debe a las personas que forman parte de nuestro equipo. Por eso, si tienes experiencia en Statistical Programming con SAS y quieres participar en proyectos internacionales