SAS Programmer I — Clinical Trials Data

A leading clinical research organization in Milan is seeking a Statistical Programmer to contribute to global clinical trials. The role involves developing analysis data sets, programming in SAS, and collaborating with international teams. Ideal candidates hold a Master's degree in Statistics or Biostatistics, have strong SAS skills, and excellent...

Job Description Please submit your CV in English. You willcontribute to statistical programming activities related to global clinical trials, work closely with international teams of statisticians, programmers and data managers, program data sets andsummaries. You will: Develop analysis data sets structure Develop program requirements and specifications Be...

Company DescriptionWe are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do.A dynamic, global company founded in ****, we bring together more than 2,700 driven, dedicated and passionate individuals.We work on the frontline of medical science, changing lives, and bringing new medicines to those who...

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Job Overview Assist in the development and implementation of solutions to global technical service issues and concerns regarding EDC or SAS or other proprietary software including proactive prevention strategies. Develop / validate Custom / Complex SDTM / SAS datasets / Listings / reports. Efficiently handle external data and data reconciliations....

Overview SR is expanding its capabilities and looking for a Senior Data Manager. Profile Requirements Degree in life science, pharmaceutical, biology or related field Previous experience in a pharmaceutical or clinical research organization (CRO) environment, at least 6 years, is required. Knowledge of aspects of clinical trials and management of clinical...

Overview SR is expanding its capabilities and looking for a Senior Data Manager. Profile Requirements Degree in life science, pharmaceutical, biology or related field Previous experience in a pharmaceutical or clinical research organization (CRO) environment, at least 6 years, is required. Knowledge of aspects of clinical trials and management of clinical...

Profile Requirements Degree in life science, pharmaceutical, biology or related field Previous experience in a pharmaceutical or clinical research organization (CRO) environment, at least 6 years, is required. Knowledge of aspects of clinical trials and management of clinical data (eCRF design, data management plan, preparation of the related documentation,...

On behalf of our Client a global pharmaceutical company, IQVIA is looking for a Lead Statistical Programmer who can join an exciting working environment in a dynamic atmosphere. JOB DESCRIPTION: - To develop SAS programs and statistical output for the management and reporting of clinical trial data managed by GCD. - To guarantee quality of statistical...