Statistical Programmer Expert
3 weeks ago
At IQVIA, we're pushing the boundaries of human science and data science to make a meaningful impact on healthcare. As a Principal Statistical Programmer with a specialized focus on pharmacokinetics (PK) and pharmacodynamics (PD), you'll play a pivotal role in designing, executing, and analyzing clinical trials to support the development of innovative therapeutics.
Key Responsibilities- PK/PD Data Analysis: Conduct comprehensive PK/PD data analysis using statistical methodologies to inform clinical trial designs and decision-making processes.
- Statistical Programming: Develop and implement robust statistical programming solutions for PK/PD data analysis, adhering to industry best practices and regulatory standards.
- Protocol Development: Contribute valuable input during protocol development to ensure proper incorporation of PK/PD endpoints and statistical methodologies.
- Clinical Trial Support: Collaborate with cross-functional teams to deliver timely and accurate PK/PD data analysis for ongoing clinical trials.
- Education: Master's or Ph.D. in Biostatistics, Statistics, or a related field with a strong emphasis on PK and PD.
- Experience: Substantial experience in statistical programming using SAS, R, or other relevant programming languages within the pharmaceutical or biotech industry.
- Skills: Proven expertise in PK/PD data analysis and interpretation, including modeling and simulation, as well as solid understanding of clinical trial designs, protocols, and regulatory requirements.
We offer a competitive salary range of $111,400.00 - $203,100.00, depending on your qualifications, experience, and location. Additionally, you can expect a comprehensive benefits package, opportunities for professional growth, and a dynamic work environment that values innovation and collaboration.
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