Senior/ Principal Biostatistician - Remote
Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases.
We’re looking for an exceptional Senior Biostatistician or Principal Biostatistician to bring your passion to our team. You will be encouraged to grow professionally and personally while enjoying cross-functional partnerships with genuinely supportive colleagues, regardless of location or seniority. Most importantly, you will be using your skills to bring tangible hope to critically ill patients around the world.
At Premier Research, we are science-minded and heart-centered. Join us.
As a Senior/Principal level Biostatistician, you’ll have the opportunity to represent Premier Research as our primary contact with our sponsors, applying knowledge of statistics to independently provide statistical consulting, assist with study design and protocol development, and performs statistical analysis of clinical trials. You’ll review project related documents, prepare statistical analysis plans (SAPs) and statistical reports. You will also develop analysis data specifications, create analysis datasets, Tables, Listings and Graphs (TLG) of clinical trial data using SAS. In this role, you’ll perform quality control of TLGs and derived data sets created by others, as well as develop and validate SAS programs, macros, and utility tools.
You’ll also have the unique opportunity to work on NDA submissions--to engage with studies at the program level—preparing Clinical Summaries of Safety (ISS) and Efficacy (ISE).
What you’ll be doing:
- Independently utilize your respected expertise to provide statistical consulting
- Prepare statistical sections of protocols, performing sample size and power calculation for studies, and create randomization schedule per study design and relevant specifications
- Review protocols, case report forms (CRFs), data management plans, data specifications and other related study documents
- Develop statistical analysis plans (SAP) in accordance with the protocols and SAS programs to create statistical models and complete statistical analyses
- Support integrated summaries of safety and efficacy (ISS and ISE) for regulatory submissions
- Independently prepare analysis data specifications
- Develop SAS programs to create derived variables and analysis data sets and computer programs to generate listings, tables, and graphs using SAS
- Perform quality control of analysis data and TLGs
- Review and provide input in interpreting analysis result to clinical study report
You'll Need this Background to be Considered:
- Advanced degree (MS or PhD, or equivalent) in statistics or closely related field along with 4-6 years (or 3-5 years for PhD) of direct experience of clinical trials design and regulatory knowledge and analysis with advanced SAS programming experience
- Proven knowledge of CDISC standards and application of those standards to projects; demonstrated working knowledge of advanced SAS macro development and code generation/management algorithms
- Ability to effectively communicate with others on the project team and in the department; strong interpersonal communication skills
- Detail oriented, well organized with the ability to work on several projects simultaneously
- Excellent team player, collaborative and maintains a positive, results-orientated work environment
- Accountable, dependable and demonstrates strong commitment to the role
- Is customer service focused in approach to work, both internally and externally