Biostatistico - Swiss Cro

1 settimana fa


Como, Italia Page Personnel Italia A tempo pieno

Designs, analyzes, implements, and reports findings on targeted statistical research studies; provides consultation to investigators and researchers on experimental design and statistical research approaches, requirements, and scientific standards to advance medical knowledge and improve research in public health.
- Works with investigators to formalize analysis plans and reporting specifications; advises to choose of statistical analysis strategies, reliability of measurements and identifiability of models, and interpretation and presentation of statistical results.
- Assists in the preparation of clinical trial documents and reports, protocols, investigator brochures, scientific abstracts, peer-reviewed manuscripts, and responses to requests from regulatory agencies, local Institutional Review Board, and other health authorities.
- Reviews and analyzes safety reporting, biomarker analyses and other aspects of clinical trial monitoring.
- Plans and documents computer data file structure; develops, programs, manages, and maintains complex statistical databases; performs or supervises data entry.
- Uses a variety of advanced statistical software, methods, and techniques to gather, analyze, and interpret research data to derive useful information for research data; advises and assists in the development of inferences and conclusions, as appropriate.
- Develops enhancements to statistical software, as appropriate, by programming new techniques; maintains knowledge of current and emerging trends in statistical analysis methodology.

Fast growing company|Medical Devices and Pharmaceuticals

Master's Degree in scientific disciplines or equivalent experience

Atleast 3 yearsofprofessionalexperience in theroleofBiostatistician in CRO or PharmaceuticalIndustries

Swiss CRO based near to the Italian border

Permanent swiss contract

For a Swiss CRO I'm looking for a Biostatistician


  • Cra - Swiss Cro

    1 settimana fa


    Como, Italia Page Personnel Italia A tempo pieno

    Conducting site qualification (SEV), site initiation (SIV), interim monitoring (MOV) and close-out visits (COV), documenting the activities carried out, ensuring regulatory, ICH-GCP guideline, protocol and SOPs compliance. - Responsible to evaluate and supervise site and staff performance, providing adequate and specific training based on ICH-GCP...