.Principal Biostatistician (EMEA Only - Medical Affairs) Updated: December 9, 2024Location: Spain-Europe - ESP-Home-Based (Barcelona)Job ID: 24006630 Principal Biostatistician (Medical Affairs) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Job Responsibilities Specific to role: Support complex analysis for Publication Reviewing abstract, posters, manuscripts Strong communication, challenge the medical, make good proposal, collaborate Basic programming in SAS and/or R required Observational studies (propensity score, causal inference, etc.) experience beneficial Experience in RWE is acceptable Study and project planning beneficial Experience in clinical trials would be good to have Experience in HTA/HEOR – present for additional position if such candidates are identified General: Serves as a statistical department resource, mentors biostatisticians on job skills, and oversees or develops training plans or materials for Biostatistics associates. Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high quality work. Provides support across all statistical tasks during the lifecycle of the project, from protocol to CSR. Prepares or oversees the preparation of Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures. May be responsible as Lead Biostatistician for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report. Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis. Implements company objectives, and creates alternative solutions to address business and operational challenges. As biostatistics representative on project teams, interfaces with other departmental project team representatives. Conducts and participates in verification and quality control of project deliverables. May lead complex or multiple projects (e.G