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Looking for an experienced person who has worked in the area of new drug development. We have a need for someone who understands
the entire process that can help in a consultant role to setup the file and data management systems for both data and files to help
in the long term maintenance of documents used throughout the process. You would serve in an advisory role for our technology partner.
Requirements
7 to 10 years as a scientist or clinical director during the development of a drug
Very experienced in typical drug treatment cycle and processes
Can serve in an advisory role
Able to help establish document and data controls: naming conventions, retention policy, etc
Strong awareness of what will be needed for different regulatory agency
This is a part-time contract role
This can be done partially off hours from your full time job
Remote work is ok
Must be a US citizen and able to pass a background check
Please respond with expected rates and a resume.