Creative Biostatistician

The work often involves cooperation with colleagues at our other offices.You will be a member of the Study Team which is responsible for the planning, performance, report and documentation of statistical tasks during the study process, according to company policies, SOPs and regulatory requirements. We are now looking for another experienced Biostatistician who, like ourselves, appreciates a flexible working environment filled with interesting assignments and who enjoys working with highly competent colleagues in a small dynamic group.The position is full-time and you will be located at our office in Lund, Sweden.The main responsibilities of the Biostatistician will include: .Providing input to all sections of a study protocol (i.e.study design) .Writing statistical analysis plans .Writing statistical reports, and contributing to clinical and integrated reports .Contact with clients in questions regarding statistical issues in projects .Reviewing and contributing to Standard Operating Procedures (SOPs) within statistics .Contributing to other SOPs .SAS programming for the analysis of a clinical study (including summary statistics and statistical testing) Qualifications: .Academic degree in mathematical statistics or statistics on at least B.Sc.level .Skills in written and spoken English .Good communication and management skills Other requirements preferred: .Two years experience of clinical studies as a statistician .Knowledge of external guidelines within the area .