EMPRESA:
BIOKIT, SA, empresa de biotecnología ubicada en el Vallés Oriental, perteneciente al grupo empresarial Werfen Group, desea incorporar a su departamento de I+D un bioestadístico/a.
La actividad principal de Biokit es la investigación, producción y comercialización de reactivos de diagnosis in vitro de enfermedades infecciosas, proteínas séricas y transtornos de la coagulación.
Adjuntamos a continuación resumen, funciones y requisitos solicitados para la posición ofrecida
RESUMEN
This position requires innovative technical statistical expertise, strong communication skills, effective experimental design I data analysis strategies, and "fit-for-purpose" implementation capability applied to solve problems for internal systems and processes. The resulting work will lead to more effective scientific learning and better evidence-based decision-making from data. This role is integrated within projects to provide a greater understanding and insights from data which will provide, clearer, defensible, and timely data-driven actions, accelerating successful project completion.
PRINCIPALES FUNCIONES Y RESPONSABILIDADES:
- Lead the development of company standards and increasingly efficient processes for statistical activities.
- Provide statistical data analysis matched to purpose. Leverage data visualization, holistic multivariate analysis and nonstandard approaches to deliver additional insights and scientific understanding, where potentially beneficial and exploitable.
- Provide support for continuous improvement activities for R&D, QC and manufacturing through the application of statistical methods to improve product quality, cost, and delivery.
- Provide support for short-term problem solving activities for R&D, QC, and manufacturing through the application of statistical methods to improve product quality, cost, and delivery.
- Deliver and communicate results succinctly to the team and other appropriate audiences through formal and informal presentations
- Participate in the design and review of clinical protocols, including preparation of statistical sections, sample size calculations, randomization, and study design recommendations.
- Participate in efficacy and safety analyses for clinical trials data.
- Work closely with Scientists databases management.
FORMACIÓN ACADÉMICA Y HABILIDADES:
- PhD in statistics with 3 years or MS with 6 years of experience preferable in IVD or pharma industrial settings.
- Demonstrated leadership and self-direction.
- Demonstrated experience in data analysis, predictive modeling and experimental design.
- Ability to draw conclusions from data and recommend actions.
- Ability to explain statistical concepts to non-statisticians.
- Expertise in statistical software (R, S-Pius, SAS, or similar).
- Experienced user of Office Package (Excel, Word, PowerPoint).
RECEPCION CV:
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