With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro
A global pharmaceutical company in Milan is seeking a Statistical Programmer to support the programming of outputs for clinical studies. This role requires a scientific degree and 3-5 years of experience in a CRO or pharmaceutical company.
Etablissement : FIDEMECA Type de contrat : CDI Temps de travail : Temps plein Lieu: Sainte-Florence FIDEMECA, qui sommes-nous ? Passionné par le contrôle et la précision ? Jouez un rôle clé dans le contrôle et
IQVIA Laboratories is looking for a Lead Programmer (Centralized Monitoring Analyst) in Rome, Italy. The role requires at least 3 years of relevant experience in pharmaceutical research and a minimum of 2-3 years of SAS programming experience. You
ResponsibilitiesAccountable for driving achievement of project milestones from study start‑up through to delivery of the database and monitoring of time spent on tasks.Provide Database Programming input into protocol data collection assessments.Create the annotated CRF (aCRF) using
Experteer Overview As Principal Database Programmer, you lead the Database Programming (DBP) team and shape the clinical database to capture study data from paper and electronic CRFs. You develop data checks (SAS and otherwise), ensuring accurate, complete data
Experteer Italy is looking for a Biostatistics Project Lead to drive statistical activities for global clinical trials. In this role, you will coordinate with teams of statisticians and programmers, design analysis plans, and ensure the accuracy of
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary.This role is part of a sponsor dedicated
Experteer Italy is seeking a Principal Database Programmer in Verona, Italy. In this role, you will lead the Database Programming team, ensuring accurate and complete data delivery while aligning with scientific needs. You will also influence strategy
Experteer OverviewIn this Biostatistics Project Lead role, you drive statistical activities for global clinical trials and coordinate with cross-functional teams of statisticians, programmers, and data managers. You design analysis plans, review deliverables, and lead SAS-driven analyses including interim,
Experteer Overview In this role you will lead statistical activities for global clinical trials, collaborating with international teams of statisticians, programmers and data managers. You will design and review analyses, SP/ADA procedures, and QA statistical deliverables while
Experteer OverviewIn this role you will drive statistical activities for global clinical trials and lead SAS programming teams. You will coordinate with statisticians, data managers and vendors to deliver analyses, SAPs and datasets that meet CDISC ADaM
Job Description You will contribute to statistical activities related to global clinical trials and work closely with international teams of statisticians, programmers and data managers, including the role of biostatistics project lead. In this role, you will: