CPMS CPAQ Associate - The Steely Group
Hybrid, CA 91320
About the Job
This position is part of the Clinical Pharmacology Modeling & Simulation (CPMS) group. The individual in this position will be responsible for pharmacokinetic-pharmacodynamic (PK-PD) data review, data modification and analysis through specialized software and macros, drafting reports, coordinating timelines across functions, and generating datasets.
Quality control (QC) of data, tables/figures/listings, and text to ensure accuracy and consistency with supporting documentation will also be a key responsibility. Other duties include archival and other projects as needed.
Requirements / Qualifications:
Quality control (QC) of data, tables/figures/listings, and text to ensure accuracy and consistency with supporting documentation will also be a key responsibility. Other duties include archival and other projects as needed.
Requirements / Qualifications:
- This position requires a BS or MS degree in biological sciences, strong verbal and written communication skills, good organizational skills, meticulous attention to detail, and the ability to handle multiple projects simultaneously.
- 0-2 years of experience (Academia or Post Grad - any industry)- degree in life sciences or math preferred
- Strong analysis and software (eg, excel) skills
- Good analytical and writing skills
- Good attention to detail
- Good communication
- Prior experience with data analysis and/or programming in R/SAS is ideal but not required, with a preference of experience in scientific research fields.
Source : The Steely Group