Clinical Trials Project Manager

Written by lmorrell - - Comments Off on Clinical Trials Project Manager
UCLA Health
Published
March 29, 2021
Location
Los Angeles, California
Job Type

Description

 

Researchers adjust VR suit on patient

 

Clinical Trials Project Manager

 

Summary Information
Posting Category:
Research
Work Location:
USLos Angeles, CA
UCLA Title: 7261-PUBL ADMSTN ANL PRN
Job #: 13453
Work Hours:
M-F 8:00 am to 5:00 pm
Job Type: contract
Duration: 12 month contract
Salary Range:
$63900.00 – $126400.00 Annual
Layoff Referral Deadline:
4/8/2021
Bargaining Unit:
99
Posted Date:
March 25, 2021

Overview

You can find the cures you know are out there. At UCLA Health, you make it happen as part of a groundbreaking Research team, working to understand hundreds of medical disorders and improving processes for dozens of procedures across the globe.

 

 

 

 

 

 

 

 

Qualifications

  • Bachelor’s degree in science or health related field strongly preferred
  • 5 or more years in laboratory/project management setting.
  • Knowledge in the following laboratory procedures and instruments:  clinical chemistry, hematology, microbiology, virology, and immunology.
  • Thorough understanding of Good Laboratory Practices (GLP)/ Good Clinical Laboratory Practices (GCLP) and CLIA regulations.
  • Ability to recognize deviations from expected and/or normal results;  analyze results for possible solutions;  recommend new test methodologies and/or modify existing ones to achieve desired results; evaluate new laboratory techniques;  prepare and analyze a variety of data;  provide detailed documentation and analysis of clinical research data.
  • Ability to organize and direct the daily activities of participating laboratories; participate with supervisor in work planning, staff training, evaluating work, and counseling; evaluate quality control procedures; review work of others for conformance with quality control procedures; maintain quality control records; perform safety checks; ensure compliance with health and safety guidelines.
  • Ability to develop and provide instruction and training for staff at international laboratories in performance of laboratory procedures including total quality management.  Ability to develop necessary training tools to assist laboratories (i.e., checklists, training materials, etc.).
  • Working knowledge of assay validation, quality assurance and quality control procedures and properly documenting laboratory processes and procedures as well as corrective actions and preventative actions (CAPA).
  • Experience working with laboratory data/information management systems or laboratory database would be beneficial.
  • Medical technologist degree or prior experience implementing clinical research testing is a plus.

 

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