Dr. Irene Santi

Developing study protocols (input to statistical sections, reviewing) Preparing Statistical Analysis Plans (SAP) Determination/justification of power and sample size for different clinical trials Assistance in optimizing quality standards and SOPs related to medical statistics. Reviewing work of other biostatisticians Providing support and consultancy to clinical colleagues and to other statisticians on various statistical aspects of clinical trials, as needed.

Data collection of relevant clinical information Collaborate, as a study team member, with different cooperation partners (clinics, population registries and health registries) Administration of all different data in a Microsoft Access database. Statistical analysis using SAS and STATA, applying both newly implemented methodologies and standard analytical procedures. Participate in various national and international workshops and conferences.

Worked in Molecular Genetic Epidemiology department, analyzing the Swedish Family Cancer Database to determine clinical, environmental and genetic factors as prognostic of gastrointestinal cancers. In particular: · Data managing to collect the relevant information for the study · Statistical analysis using SAS · Present results in various national conferences.

Involved initially in an epidemiological surveillance program to investigate in particular CNS tumors and hematological malignancies. Later involved in a case-control study on leukemia and NH lymphoma. This position included: · Collaborating with clinics and health-related offices · Data management: entry, screening, editing and auditing · Statistical analysis using SAS

Cancer epidemiology.

Post graduate specialization in medical statistics.