CPMS TPU Associate (JP5108)

Location: Thousand Oaks, Ca
Date Posted: 12-10-2018
Job Title:  Entry Level CPMS TPU Associate (JP5108)
Location: Thousand Oaks, Ca.
Type: Contract
Duration: 12 months with possible extension
Business Unit: Clinical Pharm Modeling & Simulation
Rate: $15-18/Hour
 
3Key Consulting Inc. is recruiting for an entry level CMPS TPU associate with educational degree in
life sciences, biochemistry, biomedical engineering or related field. for a global, CA-based, bio-pharmaceutical company.
 
JOB DESCRIPTION:
The Clinical Pharmacology Modeling & Simulation (CPMS) group at Amgen, 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.
 
MUST HAVE TOP 3 SKILL SETS:
  • BS or MS in life sciences, biochemistry, biomedical engineering, or related field,
  • oral and written skills (well written resume),
  • past experience working with teams.  
Day to Day Responsibilities:
Training and reviewing SOPS and quality control of data. 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.
 
Employee Value Proposition:  To gain experience in all stages of the clinical drug development life cycle.
 
Red Flags: Discrepancies on resume in respect to work history or academic background’
 
Interview Process:  Phone and In-Person
 
 
Regards,
 
3KC Talent Acquisition Team
 
 
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