We are looking to add several additional CSV Auditors to our team for a few new clients in the US. If you are already in our system and doing work for Advarra, please simply send an email to the address below. If you have not worked for us yet, please send an email and we can start the process to get you preapproved for our robust program. Either way, we look forward to hearing from you.
The Consultant should have the following:
- Minimum of ten (10) years of Quality Assurance and/or GxP (e.g., Clinical, Manufacturing, Laboratory, etc.) experience in pharmaceutical, biotech, medical device, and other applicable life science industries
- Minimum of five (5) years of Quality Assurance experience and knowledge in Clinical, Laboratory, Manufacturing, and/or Pharmacovigilance experience
- Strong skill in interacting with clients
- Ability to work effectively with internal and external stakeholders
- Must be able to communicate effectively, both orally and in writing; write and edit written materials, explain complex information clearly and concisely in English is required.
If you are interested in this role, please include the “Job Title and Your Name” in the subject line along with your CV, and email consultingjobs@advarra.com.