
10,000+ employees
đĽ Healthcare
đź Consulting
đŚ 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.
đ September 23
Where this job comes from
Posted on Syneos Health's careers page â, not through a job board
First seen by Remote Rocketship September 23
Still open on Syneos Health's site. Checked October 30.

10,000+ employees
đĽ Healthcare
đź Consulting
đŚ 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.
⢠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 ⢠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 and adapt workloads to changing priorities ⢠Develop specifications for datasets and outputs of varying complexity ⢠Anticipate and address programming issues and define variables for peer review and sponsor/requestor acceptance ⢠Prepare for and conduct internal meetings, distribute information and minutes, and follow action items through completion ⢠Negotiate 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 review, feedback, and guidance ⢠Transfer deliverables and perform other assigned duties
⢠Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience ⢠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 summary tables, data listings, graphs, and derived datasets ⢠Knowledge of statistical analysis plans, programming specifications, annotated CRFs, and SAS database design ⢠Knowledge of applicable 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 participate in sponsor, kickoff, and bid defense meetings ⢠Ability to manage multiple projects, schedules, priorities, and deadlines
⢠Career development and progression ⢠Supportive and engaged line management ⢠Technical and therapeutic area training ⢠Peer recognition ⢠Total rewards program ⢠Inclusive culture ⢠Minimal travel may be required
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