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Position: Biostatistician 80-100%
Institution: Schweizerische Arbeitsgemeinschaft für Klinische Krebsforschung
Location: Bern, Switzerland
Duties: Ensure sound statistical planning, analysis, reporting, and publication of clinical trials and the associated research projects (e.g. translational research, quality of life, etc.). Provide statistical support and advice to other biostatisticians within the Statistics Unit and upon request to the SAKK Board, Project Groups, etc. Discuss and develop trial proposals with investigators. Review relevant documents (e.g. trial proposals, statistical analysis plans, clinical study reports, etc.). Work with Clinical Data Managers and Statisticial Programmers to ensure high data quality
Requirements: Ph.D. or Master’s Degree/Diploma in statistics or a related field with at least 3 years of experience in clinical trials; experience in oncology would be advantageous Knowledgeable in trial design, survival analysis and mixed models. Proficient in SAS; experience in R or S-Plus would be advantageous. Strong problem solving skills and ability to work both independently and in interdisciplinary teams. Very good project management skills. Excellent written and oral communication skills in English; ability to understand basic German
   
Text: The Swiss Group for Clinical Cancer Research (www.sakk.ch) employs more than 70 cowork- ers at the SAKK Coordinating Center in Bern. According to our vision âWe bring progress to cancer careâ we are a non - profit organization conducting clinical trials in oncology since 1965. We are looking to expand our Statistics Unit as per September 1 st 2018 or upon agreement with a motivated and reliable Biostatistician 80 â 100 % Your Tasks: ï· E nsure sound statistical planning, analysis, reporting , and publication of clinical trials ï· Provide statistical support and advice to other biostatisticians wit hin the Statistics Unit and upon request to the SAKK Board, Project Groups, etc. ï· Discuss and develop trial proposals with investigators ï· Review relevant documents (e.g. trial proposals, statistical analysis plans, clinical study reports, etc.) ï· Work with Clinical Data Managers and Statisticial Programmers to ensure high data quality ï· Keep abreast of developments in statistics and oncology through literature review, ï· Initiate and perform methodological r esearch in medical statistics when appropriate Requirements: ï· Ph.D. or Masterâs Degree / Diploma in statistics or a related field with at least 3 years of experience in clinical trials; e xperience in oncology would be advantageous ï· Knowledgeable in trial design, survival analysis and mixed models ï· Proficient in SAS ; experience in R or S - Plus would be advantageous ï· Strong problem solving skills and ability to work both independently and in interdisci- plinary team s ï· Very good project management skills ï· Excellent written and oral communication skills in English ; a bility to understand basic German What we offer: You will perform relevant work to contribute to clinical cancer research. We offer a friendly and modern work environment close to the ma in station, annual working time and very good social benefits. Please send your documents (CV and list of three references ) electronically (in PDF) to contact@sakk.ch (subject â statistician â) or to SAKK Coordinating Center, Stéphanie Mohler Head of Human Resources, Effingerstra sse 33, 3008 Bern . For more i nformation, you may contact Dr . Peter Brauchli, CEO ( 41 31 508 41 71 ).
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