Biostatistician/SAS-programmer

TFS Trial Form Support Global Biometrics is a global organisation with staff in both the Nordic region as well as in Central and South Europe.Our Nordic Biometric department today includes 3 SAS-programmers, 4 Biostatisticians, a Clinical Data Associate Coordinator, an Electronic Data Capture Coordinator and 5 Clinical Data Managers. We are now looking to increase the staff with another Biostatistician or SASprogrammer 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.You will be a member of the Study Team which is responsible for the planning, performance, report and documentation of statistical tasks according to company policies, SOPs and regulatory requirements.It is a permanent full-time position and it will be located at our Nordic HQ in Lund, Sweden.The start date will be 1st of December or asagreed. The main responsibilities of the Biostatistician will include: - Providing input to all sections of a study protocol (i.e.study design, sample size calculations) - Writing statistical analysis plans - Define appropriate methods for statistical analysis - 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) Requirements/Qualifications: - Academic degree in mathematical statistics or statistics on at least B.Sc.level - Skills in statistical programming, preferably SAS - Skills in written and spoken English - Good communication and management skills Preferred requirements: - Two or more years experience of clinical studies as a statistician - Good understanding of the total concept of clinical studies The main responsibilities of the SAS-programmer will include: - Responsible for programming activities within assigned studies to produce: o Consistency checks/Data checks o Subject data listings o Summary tables o Graphics Requirements/Qualifications: - Degree in system analysis or equivalent training/experience on at least B.Sc.level - Good knowledge of SAS/BASE and SQL - Good knowledge of database structure and terminology Preferred requirements: - Two or more years experience of clinical studies as a SAS programmer - Knowledge of SAS/GRAPH - Good knowledge of other relevant software - Skills in written and spoken English - Basic education in statistics and/or knowledge of SAS/STAT - Experience with CDISC TFS Trial Form Support will offer: A dynamic and growth oriented organization with a work environmentdistinguished by professionalism, integrity and responsibility.Welcome to join us and to contribute in placing TFS Trial Form Support among the top 10 worldwide CROs. We practice a continuous selection procedure, so please submit your application via the link provided on our website, http://www.trialformsupport.com/about/jobs/vac_se.htm