Updated : September 10, 2025
Location : Madrid, Spain
Job ID : -OTHLOC-3529-2DMAD-2DR
Overview
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 centers the customer and the patient, and we aim to simplify and streamline our work to be easier to work with and for. We operate in Functional Service Provider partnerships or Full-Service environments, collaborating with teams to accelerate the delivery of therapies and change lives.
Discover what our 29,000 employees, across 110 countries already know : WORK HERE MATTERS EVERYWHERE
Why Syneos Health
- We develop our people through career development and progression; supportive management; training; peer recognition and total rewards.
- We maintain a Total Self culture that unites us globally and focuses on taking care of our people.
- We value diversity of thoughts, backgrounds, cultures, and perspectives to create a sense of belonging.
Job Responsibilities
Study lead for 1-2 protocols in late phase (phase 2-3); for phase 3, may support another main statisticIRT, eCRF, DMC setup, SRMP preparationPrepare SAPs, tables, listings and figures (tfls); review specificationsSTS (statistical surveillance) and blinded data review; participate in 2-3 STS meetings during study lifeAssess data, review intercurrent events, and apply SAS or R; may partially program efficacy analysesProvide support across all assigned statistical tasks from protocol to CSR; coordinate activities of other biostatistics / programming personnelPrepare and review programming specifications for analysis datasets, tables, listings, and figures; review SAS annotated CRFs and database designEnsure data capture supports protocol criteria and planned analyses; verify quality and readiness for inspectionLead or participate in integrated analyses; attend regulatory agency meetings or respond to questions as neededFollow SOPs, work instructions, and regulatory guidelines (e.g., ICH); maintain documentation and verification / quality controlMentor other Biostatistics staff; support business development activities such as proposals and sponsor meetingsMay participate in Data Safety Monitoring Board / Committee activitiesMay lead projects and manage timelines across multiple studiesMay provide statistical programming support as neededOther duties as assigned and minimal travel may be required.
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 studies across 73,000 sites and 675,000+ trial patients. We are committed to an inclusive culture and encouraging initiative and innovation in a dynamic environment.
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