Job Title:
Principal Statistical Programmer
Company:
Syneos Health®
Company Overview:
Syneos Health® is a fully integrated biopharmaceutical solutions organization that combines clinical development, medical affairs, and commercial capabilities. With over 29,000 employees in 110 countries, it is focused on accelerating customer success by delivering modern, integrated, and data-driven healthcare solutions.
Why Syneos Health:
Strong commitment to career development and progression
Supportive line management
Training in technical and therapeutic areas
Peer recognition and rewards programs
Inclusive “Total Self” culture
Diverse and global workplace
Job Responsibilities:
Use SAS or other software to program summary tables, data listings, graphs, and datasets
Ensure output quality and adherence to project requirements
Perform validation programming and resolve discrepancies with the project team
Keep the team updated on programming status and issues
Follow relevant SOPs, WIs, and regulatory guidelines (e.g., ICH)
Maintain complete and inspection-ready documentation
Manage priorities across multiple projects; reorganize workload as needed
Develop specifications for datasets/outputs; anticipate and resolve programming issues
Lead internal meetings and ensure clear communication and follow-through
Lead statistical programming activities and monitor junior programmers
Review project documentation (e.g., SAP, CRFs, mock shells) and provide feedback
Represent programming in sponsor/kickoff/bid defense meetings
Mentor junior programming personnel; develop and present training materials
Serve as a technical expert on CDISC and other industry standards
Conduct compliance reviews of deliverables (e.g., SDTM, ADaM, DEFINE.XML)
Participate in industry standards organizations and share updates with the department
Transfer deliverables as needed
Perform other related duties
Minimal travel required
Qualifications:
Undergraduate degree (scientific or statistical discipline preferred), or equivalent education/experience
Extensive SAS programming experience in a clinical trial environment
Demonstrated ability to lead global and complex projects
Strong knowledge of CDISC standards and regulatory submission requirements
Experience mentoring others on CDISC and clinical trial processes
Excellent written and verbal communication skills
Fluent in English
Additional Information:
Duties and responsibilities may change based on business needs
Equivalent skills or education may be considered
This is not an employment contract
Compliant with ADA and EU Equality Directive
Reasonable accommodations will be provided when appropriate
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Hajipur | Patna |Kerala :
Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
Pondicherry (Puducherry) |Jharkhand :
Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Wisconsin :
Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
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Wavre |Tipperary :
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Donegal |Meath :
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Galway |County Dublin :
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China | Quarry Bay |Liaoning :
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Netherlands |Remote Australia :
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Japan | Saitama |Tokyo :
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