logo

View all jobs

CPMS CPAQ Associate

Thousand Oaks, CA
Top 3 Must Have Skill Sets:    

hard skills
Data Analytics experience
Quality Control
Report writing

soft skill: R experience

DAY TO DAY RESPONSIBILITIES / FIRST 30 DAYS: 

Training and reviewing SOPS and quality control of data.

The Clinical Pharmacology Modeling & Simulation (CPMS) group at Thousand Oaks, CA, is looking for a contingent worker for a 12-month contract. 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. 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. 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.

Education: Bachelors degree - life sciences, biochemistry, biomedical engineering, or related field

"This posting is for Contingent Worker, not an FTE"

More Openings

Project Manager Senior
Scientist

Share This Job

Powered by