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Senior Statistical Programmer

unlimited holidays - extra holidays - extra parental leave - long remote period allowed
Remote: 
Full Remote
Experience: 
Senior (5-10 years)
Work from: 
United States

Offer summary

Qualifications:

BS in Stats, Math, Computer Sciences, Solid SAS Programming Experience.

Key responsabilities:

  • Plan, develop, execute programs in SAS.
  • Provide programming expertise for clinical trials.
  • Review, validate, and document statistical programs.
  • Perform data analysis in collaboration with statistician.
Katalyst HealthCares & Life Sciences logo
Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/
51 - 200 Employees
About Katalyst HealthCares & Life Sciences
Katalyst Healthcare's & Life Sciences (Katalyst HLS) is a Global Contract Research Organisation that provides End-to-End Clinical Research Services for Healthcare and Life Sciences companies globally. At Katalyst HLS offers ICH-GCP compliant clinical trial services from Phase I–IV in all key therapeutic areas to support clinical development and research requirements and also provides validation, quality and regulatory services for Pharma/Bio-Pharma/Medical Device industries. Services:- Clinical Trial Management- Clinical Data Management- Biostatistics & Statistical Programming- Medical Writing- Pharmacovigilance- Quality and Regulatory Affairs- GMP, GLP and GCP Validations- Manufacturing Process Validations- Equipments & Instruments Validations- Computer Systems Validations- Human Resourcing
See more Katalyst HealthCares & Life Sciences offers

Job description

Resposnsibilities:
  • Plan the execution of programs in statistical programming languages within project. Develop, test, validate, document, maintain and execute programs in SAS.
  • Provide programming expertise for clinical trials in programming, documentation, validation and review of summary tables, data listings, and graphs for inclusion in clinical reports or presentations in collaboration with project statistician.
  • Review and validate statistical programs and ensure that all appropriate program validation documentation to meet regulatory and company standards are consistently structured to permit efficient programming, reporting, and review.
  • Perform analysis in response to data requests in collaboration with designated statistician.

Requirements:

  • BS in Stats, Math, Computer Sciences.
  • 8+ years of Experience working within Medical Device/Pharma/Biotech Solid SAS Programming Experience.
  • Excellent understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device setting.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Hard Skills

Data AnalysisClinical TrialsSAS MacrosStatistical Programming
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