Job Description

Job Code:

Torrance, US-CA  90502

Employment Status:
Part-time position; work less than 30 hours per week (no benefits)

# of Openings:


Minimum education requirements:
Other (Specify)

Salary Range:

Last Updated:
6/11/19 4:24 PM

  • Managing all aspects of investigational product preparation, distribution and reconciliation
  • Complying with SOPs, GCP, GPP, study protocols, and any applicable State or Federal regulations to ensure the efficient and compliant operation of the Pharmacy
  • Maintain close cross-functional relationships with clients and the clinical team to best design, plan, implement and direct IP activities to best meet the clinical objectives
  • Assisting the clinical team with study-related activities such as protocol review and developing study manual for drug preparation
  • Coordinate quality assurance activities relative to drug inventory, preparation, and other activities related to GMP, GCP, and ICH guidelines
  • Ensuring that IP is stored in compliance with the protocol
  • Ensuring that IP is correctly prepared and labeled for dosing in a manner that is in strict compliance with the study protocol, randomization code, SOPs and any other applicable regulations
  • Ensuring availability of sufficient test and reference products for study execution, as appropriate
  • Working with clients in identifying critical issues relative to IP preparation and administration, and presenting possible solution(s)
  • Participate in sponsor monitoring visits relative to project IP documentation and accountability, as requested
  • Ability to work creatively in a fast paced environment
  • Other responsibilities, as assigned


  • Doctorate of Pharmacy 
  • 5+ years of experience in an inpatient, academic or research environment 
  • Detail oriented a MUST

Application Instructions

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