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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:

Proficiency in Base SAS, SAS/STAT , SAS Macro language, Experience with STDM and ADaM datasets preferred.

Key responsabilities:

  • Contribute to analysis plans and integrated clinical reports
  • Ensure compliance with standards, quality assurance procedures
  • Develop and maintain software systems, assist in data integration
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

Responsibilities:
  • Contribute to the preparation of analysis plans.
  • Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical, statistical reports and other similar reports.
  • Contribute to the integrated clinical/statistical report and other similar documents.
  • Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting.
  • Perform quality assurance procedures on work performed by others.
  • Develop, test, validate, document, maintain and execute software and/or systems using the currently endorsed tools or support of production activities
  • Assist in the integration of data from remote entry sites.
Requirements:
  • Proficiency in Base SAS, SAS/STAT and SAS Macro language.
  • Demonstrated ability to work in teams to deliver critical milestones.
  • Experience with STDM and ADaM datasets, tables, listings and figures preferable.
  • Excellent verbal and written communication skills.
  • 5-7 years of experience with a biotech, pharmaceutical company, or CRA/CRO.

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

SAS MacrosSAS/STATBase SASStsadmDataset

Other Skills

  • Verbal Communication Skills
  • Teamwork
Are you interested?

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