For an international tobacco company in Neuchâtel, we are seeking a :
Location : Neuchâtel
Start date : 1st of April
Contract duration : 1 year
Independently apply statistical practices,procedures and / or theory to design, conduct, and report pre and post-market clinical studies conducted to assess risk profile of alternative products to cigarettes.
Work closely with other functions to answer important questions and apply industry standards to tobacco products by translating strategic needs to innovative statistical solutions.
Responsible for ensuring timeliness, quality and completeness of the statistical deliverables for assigned clinical Studies according to appropriate regulatory framework.
Ensuring the results from clinical Studies are reported accurately in a manner that ensures the integrity of the statistical analyses.
Interaction with the Clinical Research Organization in charge of the study for all statistical aspects including follow-up of budget related to statistical activities.
Responsible for the statistical resources working on allocated clinical Studies.
Skills and Competencies needed :
Work Experience :
10+ years of relevant experience in study design, conduct, and analysis of clinical studies in pharmaceutical, consumer goods, or clinical research environments.
Functional skills :
Experience with SAS is required.
Knowledge of CDISC (SDTM, ADaM) standards is required.
Experience with Phoenix WinNonlin®, NONMEM, and R is a plus.
Experience interacting with US and / or international health authorities is a plus.
Excellent interpersonal communication, organizational and leadership skills with an ability to work both independently and in a team environment.
Please note a valid Swiss work permit or Swiss or EU-25 / EFTA citizenship is required for this position