Updated: September 10, 2025
Location: Madrid, Spain
Job ID: 25101674-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 statistic
IRT, eCRF, DMC setup, SRMP preparation
Prepare SAPs, tables, listings and figures (tfls); review specifications
STS (statistical surveillance) and blinded data review; participate in 2-3 STS meetings during study life
Assess data, review intercurrent events, and apply SAS or R; may partially program efficacy analyses
Provide support across all assigned statistical tasks from protocol to CSR; coordinate activities of other biostatistics/programming personnel
Prepare and review programming specifications for analysis datasets, tables, listings, and figures; review SAS annotated CRFs and database design
Ensure data capture supports protocol criteria and planned analyses; verify quality and readiness for inspection
Lead or participate in integrated analyses; attend regulatory agency meetings or respond to questions as needed
Follow SOPs, work instructions, and regulatory guidelines (e.g., ICH); maintain documentation and verification/quality control
Mentor other Biostatistics staff; support business development activities such as proposals and sponsor meetings
May participate in Data Safety Monitoring Board/Committee activities
May lead projects and manage timelines across multiple studies
May provide statistical programming support as needed
Other 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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