
10,000+ employees
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą Logistics
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
đ„ 10 minutes ago
Where this job comes from
Posted on Syneos Health's careers page, not through a job board
First seen by Remote Rocketship 10 minutes ago

10,000+ employees
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą Logistics
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
âą Use SAS or other software to develop custom programming code for summary tables, data listings, graphs, and derived datasets according to statistical analysis plans and programming specifications âą Ensure outputs meet quality standards and project requirements âą Perform validation programming and resolve discrepancies with Programmers, Biostatisticians, and project team members âą Maintain complete, current project documentation, testing, and quality-control materials for inspection readiness âą Manage schedules and priorities across multiple projects âą Develop dataset and output specifications according to statistical and sponsor requirements âą Prepare for and conduct internal meetings, distribute information and minutes, and track action items âą Negotiate time estimates and complete study programming activities within allotted timelines âą Act as lead statistical programmer, direct programming activities, and monitor deliverables âą Review Statistical Analysis Plans, mock shells, programming specifications, annotated CRFs, and SAS database designs âą Participate in sponsor, kickoff, and bid defense meetings as the statistical programming representative âą Mentor programming personnel through training, work review, feedback, and guidance âą Transfer deliverables and perform other assigned work-related duties
âą Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience âą Extensive programming experience in SAS or other required software, preferably in a clinical trial environment âą Excellent written and verbal communication skills âą Ability to read, write, speak and understand English âą Ability to follow applicable SOPs, WIs, and relevant regulatory guidelines such as ICH âą Ability to manage multiple projects, schedules, and changing priorities âą Ability to develop specifications for datasets and outputs of any complexity âą Ability to lead statistical programming activities and direct other programming personnel âą Minimal travel may be required
âą Career development and progression âą Supportive and engaged line management âą Technical and therapeutic area training âą Peer recognition âą Total rewards program âą Inclusive culture âą Reasonable accommodations for applicants and employees with disabilities, when appropriate
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