Sr. SAS Programmer

Overview

Sr. SAS Programmer role at Katalyst CRO
.

• Prepare data for state-of-the-art analysis, such as PPK, PKPD, exposure-response (efficacy or safety), and C-QTc, typically based on CDISC ADaM / SDTM datasets.
• Prepare data for state-of-the-art NCA analysis, such as ADPC, PP, and ADPP, including the creation of defined packages and reviewer guides.
• Write, maintain, and develop high-quality Programs and Macros (R, SAS) to facilitate the construction of analysis datasets and P21 validations.
• Interact with members of the multidisciplinary team to establish project timelines; computerized data validation checks and ad hoc requests.
• Design and implement statistical algorithms and code in conformance with defined programming processes and standard operating procedures.
• Conduct exploratory analyses of PKPD data in support of modeling analyses.
• Write statistical analysis plan and perform exposure-analysis on QTc as requested.
• Following completion of the project deliverables, you are responsible for the creation of an electronic submission package for future submission to regulatory agencies.

• BS, MSc, Master in Statistics, Mathematics, PhD, Pharm
  
  D, or related fields.
• About 5 years' experience and expertise in PKPD programming and analysis, report writing, and regulatory drug submissions.
• General knowledge of clinical drug development and demonstrated knowledge of pharmacokinetics and pharmacology.
• Expertise in PK/PD programming with strong quantitative skills applied to develop PPK, PKPD, ER-efficacy, ER-safety, and C-QTc datasets.
• Expertise in software used for dataset construction (e.g. R, SAS).
• Strong track record of working in various therapeutic areas.
• Familiarity with regulatory requirements and trends with respect to data standards.

• Seniority level:
  Associate
• Employment type:
  
  Contract
• Job function:
  Information Technology
• Industries:
  Pharmaceutical Manufacturing