- Search jobs
- Toronto, ON
- statistical programmer
Statistical programmer Jobs in Toronto, ON
Create a job alert for this search
Statistical programmer • toronto on
Principal Statistical Programmer FSP
CytelToronto, ON, CASenior Principal Statistical Programmer - Lead & Innovate
Syneos HealthToronto, ON, CAC++ Programmer
Waterfront InternationalToronto, ON, CASenior Statistical Programmer
Everest Clinical Research Services IncToronto, OntarioLead Statistical Programmer – SAS, SDTM / ADaM Expert
Candido Consulting Group IncToronto, ON, CAPLC Programmer
ATS AutomationToronto, ON, CAPLC Programmer
ATS CorporationToronto, ON, CAAssistant Professor - Statistical Sciences
University of Toronto ScarboroughToronto, ON, CAProgrammer Analyst
USN SolutionsToronto, ON, CAQuadient Programmer
Avant Imaging and Integrated Media Inc.Toronto, ON, CACNC Programmer
Tech MahindraToronto, ON, CAProgrammer Analyst
CTECH GLOBAL LIMITEDToronto, ON, CAQuadient Programmer
AIIMToronto, ON, CAPython Developer (Statistical Analyst)
Aviva plcToronto, ON, CA- Promoted
AV Programmer
Paladin TechnologiesToronto, ON, CanadaPLC Programmer
ATS Automation Tooling Systems IncToronto, ON, CA.Net Programmer
WinsoproToronto, ON, CAProgrammer Analyst
ROSSToronto, ON, CAAudiobooks Programmer
CNSCToronto, ON, CA- Hamilton, ON (from $ 71,107 to $ 194,304 year)
- Laval, QC (from $ 99,517 to $ 192,913 year)
- Mississauga, ON (from $ 108,880 to $ 148,814 year)
- Vancouver, BC (from $ 75,507 to $ 145,000 year)
- Old toronto, ON (from $ 89,037 to $ 140,614 year)
- Toronto, ON (from $ 123,655 to $ 139,714 year)
- Montreal, QC (from $ 126,396 to $ 138,241 year)
- North York, ON (from $ 60,000 to $ 132,000 year)
- East York, ON (from $ 60,000 to $ 132,000 year)
Popular searches
Principal Statistical Programmer FSP
CytelToronto, ON, CA- Full-time
Key Responsibilities :
Provide technical leadership in SAS programs and applications designed to analyze and report complex clinical trial data in Tables, Listings, and Figures , and for electronic submissions of SDTM, ADaM datasets in CDlSC format, with minimal instruction or input from supervisor
Provide technical leadership to create, review, and approve documentation required to support data analysis, reporting, and CDlSC data submission
Ensure compliance with company SOP'S and FDA / ICH / GCP regulations
Perform quality control checks of advanced SAS code for datasets and output produced by other statistical programmers
Review, maintain study documents per standard process
Program, test, and document global utility programs and tools in accordance with standards and validation procedures
Conduct briefings and participate in technical meetings for internal and external representatives (e.g., IS, CROs, Clinical Development Partners, Software Vendors, FDA, EMA, et cetera) for projects
Perform lead duties when called upon
Perform other duties as assigned
Technical and Communication Skills :
Proven expert in all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS / STAT and SAS / GRAPH
R programming experience is a plus
Excellent and transparent communication skills and ability to interact across multiple functions
Adaptability and flexibility for when priorities change
Preferred Education and Experiences :
- MS in biostatistics or a related field, with 8+ years of experience in pharmaceutical industry, or BS in biostatistics or a related field, with 10+ years of experience in pharmaceutical industry
Cytel Inc. is an Equal Employment / Affirmative Action Employer . Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.
#J-18808-Ljbffr