Pharmaceutical Clinical QA

Edison, NJ

Job ID: 129562 Industry: CLINICAL


Pharmaceutical Clinical QA

Project Description:                                                     

Our client is a pharmaceutical company that is looking for some help in their Clinical QA department.  Currently the client has more work than their full time staff can handle and would like to supplement the team with contractors.  This person will be responsible for working with clinical protocols, clinical SOP’ s and GCP audits.


Day to Day Responsibilities:

This consultant will be coming on site part time to help the client with an abundance of work.  The consultant chosen for this role will have a strong background in GCP compliance specifically for the pharmaceutical industry.  The work will entail reviewing clinical study protocols, CSR’ s, clinical SOP’ s, clinical GCP audits, etc.  The person is joining the team because there is an abundance of work that the full time staff does not have the capacity to fulfill.

Required Skills:


Clinical QA

CSR’ s, Protocols, Audits


Job Type: Contract

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