Senior Statistical Programmer - remote

REQUIRED QUALIFICATIONS: 

• Proficiency of both R and SAS.
• Thorough understanding of clinical trial reporting process, as well as regulatory reporting requirements including electronic data submissions and CDISC implementation.
• Hands on experience programming within clinical trials and with SDTM/ADaM specifications and programming.
• Experience with the following SAS concepts: Data Step Manipulation, Merge, Sort, Transpose, Reporting (Proc Report), Comparison (Proc Compare), Error Checking (Log resolution), modeling, missing data handling approaches/procedures, figure development.
• Experience developing custom SAS macros and R functions.
• Experience with P21 reporting and DEFINE, SDRG, ADRG development.
• Base or Advance SAS certification preferred.
• In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on
• Harmonization (ICH) guidelines .
  •  Experience and knowledge of clinical data management processes and tools (Medidata Rave and Veeva preferred).
• Occasional overnight travel (2 times/year on average). 

Education/Experience:

• Bachelor’s degree or Master’s degree in:
  • programming, statistics, computer science, math, health-related sciences or other relevant field
  • 8+ years’ experience with Bachelor’s
  • 5+ years’ experience with Master’s

PREFERRED QUALIFICATIONS:

• Experience working on Phase I/II/III clinical trials.
• Experience in oncology therapeutic space.

BENEFITS:

NMDP offers regular, full-time employees medical, dental, vision, life and disability, accident/critical illness/hospital, well-being, legal, identity theft and pet benefits. Retirement, paid time off/holidays, leave and incentive plans are also offered to eligible employees. Please reference this link for more information: NMDP Benefit Information