Biostatistical Programmer

Biostatistics Research Triangle Park, North Carolina


Position at Premier Research Group Limited

Premier Research helps highly innovative bio-pharmaceutical and medical device companies transform life-changing ideas into reality. We take on the most challenging areas of study, with a special focus on unmet needs in such areas as analgesia, CNS, rare diseases, medical device and diagnostics, and pediatric research. We’re looking for a talented and energetic Biostatistical Programmer to join our team! Working at Premier Research means being an individual - you will be recognised for what you do and you will truly have an impact. You will be working in a friendly environment with colleagues who are genuinely supportive regardless of location or seniority. Premier Research is on an exciting journey - there is a true buzz throughout the company, so come and be part of it!

Company Name: Premier Research International, LLC

Position Title: Biostatistical Programmer

Location: 1 Park Dr., Suite 150, Durham, NC 27709


Summary of Duties:                            
Responsible for the production of project-related datasets, tables, listings, and figures (TLFs) required for delivery to Premier Research Sponsors.  Perform Biostatistical programming quality control and validation to support global Biostatistics projects.  Complete work through the development and validation of SAS software programs, macros, and utility tools.  Additionally, prepares specifications for data set analysis. Develop SAS programs to generate listings, tables and figures as outlined by mock TLF shells. Perform quality control (source code review, double-programming and log review) of SAS programs. Develop SAS programs to generate CDISC and other analysis data sets as outlined by respective specifications. Prepare specifications for CDISC and other analysis data sets. Assist Data Management with SAS programming needs. Keep detailed records of time spent on each project for accurate billing. Respect and maintain the confidentiality of the processed material and ensure that any regulations concerning security or confidentiality (such as the safeguarding of passwords) are complied with. Participate in efforts for efficiency and productivity in the department. Participate in corporate initiatives and actions that ensure the continued success of the company. Attend project and corporate meetings, as necessary. Duties may be performed remotely.



Bachelor’s degree in Statistics, Mathematics, Engineering, IT, or related AND two (2) years’ experience in the offered role or in Clinical Research or related roles. Experience must include two (2) years with the following: CDISC standards and application of these standards to projects; Clinical trial design and analysis principles; Data processing, database design and organization in clinical data environment; Microsoft Word, Excel, PowerPoint, and Outlook; and ICH and local regulatory authority drug research and development regulations.