Job Description

Job Description

Take your career to the next level and lead challenging study activation process on a country level. You will support clinical research teams and ensure PSI projects start smoothly and on time.

You will mainly: 

  • Lead finalization of site/vendor agreements and budgets negotiation to ensure alignment to the study activation plan
  • Customizes and prepare country- site-specific and vendor agreements and agreement amendments
  • Prepare and track the status of site and vendor agreements, budget negotiation, and coordinates the signature process
  • Additionally, you will:

  • Coordinates study startup activities with the local project team and supports all processes critical for site activation.
  • Collaborate with the project team for site activation processes
  • Assist in feasibility research and site identification
  • Collect site documents for IRB/IEC submission and/or IP-RED process
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