Clinical SAS Programmer Job at Katalyst Healthcares & Life Sciences, South Plainfield, NJ

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  • Katalyst Healthcares & Life Sciences
  • South Plainfield, NJ

Job Description

  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Job Description

  • Hands on statistical programming experience in the pharma/biotech industry
  • Strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat, and SAS Macros, preferrable experience using R. 
  • Desire to understand the disease area, protocol, SAP, and study related documents.
  • Good knowledge of clinical trial design, and statistical terminology.
  • Strong knowledge of CDISC SDTM and ADaM data models.
  • Demonstrated proficiency in developing dataset specifications, and using SAS/R to produce SDTM datasets, ADaM datasets, and TFLs.
  • Thorough understanding of clinical data structures, and data exchange with multiple data formats.
  • Expertise in performing validation of datasets, and TFLs using risk-based approach.
  • Expertise in regulatory submissions, preparation of e-sub package.
  • In-depth understanding of regulatory, industry, and technology standards and requirements.
  • Exceptional organizational, communication and time management skills, with the ability to multi-task across projects. 
  • Demonstrated ability to work in a team environment with cross-functional teams.

Qualifications

  • Strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat, and SAS Macros, preferrable experience using R.
  • Strong knowledge of CDISC SDTM and ADaM data models.
  • Demonstrated proficiency in developing dataset specifications, and using SAS/R to produce SDTM datasets, ADaM datasets, and TFLs.
  • Expertise in regulatory Submissions.

Additional Information



All your information will be kept confidential according to EEO guidelines.

Job Tags

Contract work, Immediate start,

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