
10,000+ employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • 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.
🔥 0 minutes ago
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10,000+ employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • 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.
• Develop custom programming code using SAS or other software to generate summary tables, data listings, graphs, and derived datasets • Ensure outputs meet quality standards and project requirements • Perform validation programming and resolve discrepancies with Programmers, Biostatisticians, and project team members • Maintain complete, organized, current project documentation, testing, verification, and quality-control materials • Manage schedules and time constraints across multiple projects • Develop dataset and output specifications according to statistical and sponsor requirements • Anticipate programming issues and define variables accurately for peer review and sponsor/requestor acceptance • Prepare for and conduct internal meetings, distribute information and minutes, and follow action items through completion • Establish time estimates and complete study programming activities within allotted timeframes • Act as lead statistical programmer, direct programming activities, and monitor deliverables • Review Statistical Analysis Plans, mock shells, programming specifications, annotated CRFs, and SAS database designs • Participate in sponsor, kickoff, and bid defense meetings as the statistical programming representative • Mentor programming personnel through training, work reviews, feedback, and guidance • Transfer deliverables and perform other assigned work-related duties
• Undergraduate degree, preferably in a scientific or statistical discipline; an equivalent combination of education and demonstrated programming experience may be accepted in lieu of a degree • Extensive programming experience in SAS or other required software, preferably in a clinical trial environment • Excellent written and verbal communication skills • Ability to read, write, speak and understand English • Ability to develop custom programming code for clinical trial outputs • Knowledge of statistical analysis plans, programming specifications, annotated CRFs, SAS database design, SOPs, WIs, and relevant regulatory guidelines such as ICH • Ability to perform validation programming and quality control • Ability to lead statistical programming activities and direct other programming personnel • Ability to manage multiple projects, schedules, priorities, and changing timelines • Ability to participate in sponsor, kickoff, and bid defense meetings • Ability to mentor programming personnel and develop or present training materials
• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations when appropriate
Apply Now🕒 5 days ago
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