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Clinical SAS Programmer

UNLIMITED HOLIDAYS - EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE - LONG REMOTE PERIOD ALLOWED

Remote:

Full Remote

Experience:

Senior (5-10 years)

Work from:

Offer summary

5 years of Statistical Programming experience, Bachelor's Degree in relevant field, Proficiency in SAS programming.

Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/

51 - 200 Employees

Responsibilities:

Independently develop and validate programs that generate analysis datasets based on ADaM specifications.
Prepare/QC ADaM datasets documentation: Define.xml, Reviewer's Guide and analysis metadata report.
Independently develop/validate programs that generate tables, listings and graphs specified in the protocol or the Statistical Analysis Plan (SAP) including efficacy statistical analysis.
Perform quality control on final reports.
Provide QC and validation reports.
Support development of technical programming specifications for ADaM standards

Requirements:

5 years of Statistical Programming experience in Biotechnology, Contract Research, and/or pharmaceutical industry
Bachelor's Degree in Biostatistics, Computer Science, Mathematics or Life Sciences
Strong SAS programming skills required in Windows & UNIX environment.
Proficiency in SAS/Base, SAS Macros, SAS/Stat
Experience in developing CDISC compliant ADaM specifications.
Experience in validating ADaMs and TFLs
Strong knowledge on SAS macros and able to work on modifying/existing SAS programs.
Great interpersonal skills
Excellent communication skills (written and verbal)
Strong atteniton to detail
Highly organized.
Experience with all Clinical Phases I, II, III and IV of trials.
Experience with creating PK datasets and outputs (ADPC and ADPP), generating datasets for PK analysis.
Experience in CNS.
Experience in SAS Enterprise Guide and SAS Studio