Beschreibung
Job role:
.Acting as a Study Programmer on study teams, managing your time so as to provide timely input
.Supporting the statistical reporting, including production of listing, tables and figures, for Phase II to IV clinical studies and Pharmacovigilance data
.Reviewing and monitoring data received from data management to ensure suitability for reporting
.Assisting in the design of study databases ensuring adherence to CDISC standards
.Programming of ad hoc queries on study databases
.Act as a principal SAS programming contact within the team
.Perform quality control review of work completed by other members of the team or CROs
.Interacting with report writers in the production of integrated clinical reports and other documents containing information from clinical study databases
.Ensuring successful execution of studies by liaising with other departments
.Participating in the development of departmental processes, including standard working practices, operating procedures and implementation of CDISC
Skills Required:
.Bachelor's degree in a Life Sciences field
.Proven experience as a SAS Programmer within a clinical environment
.Knowledge of applicable regulatory requirements and guidelines such as ICH Guidelines
.Proficient in the use of SAS Base (SAS/Graph and SAS/Stat would be an advantage)
.Familiar with data from clinical trials
.Training in statistics would be an advantage
.Excellent time management and interpersonal skills
.Strong attention to detail, positive, creative, good communicator