Principal Biostatistician (EMEA Only - Medical Affairs) Updated: December 9, 2024 Location: Spain-Europe - ESP-Home-Based (Barcelona) Job ID: 24006630 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.
Review abstracts, posters, and manuscripts.
Strong communication skills, ability to challenge the medical, make good proposals, and collaborate.
Basic programming in SAS and/or R required.
Experience with observational studies (propensity score, causal inference, etc.)
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 Responsibilities: Serve as a statistical department resource, mentor biostatisticians on job skills, and oversee or develop training plans or materials for Biostatistics associates.
Direct the activities of other biostatistics personnel on assigned projects to ensure timely completion of high-quality work.
Provide support across all statistical tasks during the lifecycle of the project, from protocol to CSR.
Prepare or oversee 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.
Create or review programming specifications for analysis datasets, tables, listings, and figures.
Review 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.
Implement company objectives and create alternative solutions to address business and operational challenges.
As biostatistics representative on project teams, interface with other departmental project team representatives.
Conduct and participate in verification and quality control of project deliverables.
May lead complex or multiple projects.
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