Job Summary

• Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
• Serve as the primary point of contact for investigative sites, Site Activation Managers (SAM), Project Management teams, and relevant departments regarding all contract and budget–related activities, ensuring full compliance with SOPs, WIs, and regulatory requirements.
• IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication.

Matching Summary

Skills & Requirements

Key Requirements

• Bachelor’s degree in Life Sciences, Law, or related field
• Minimum 3 years of experience in clinical research
• 2-3 years of direct experience in site contract and budget negotiations
• Demonstrated experience managing contract/budget negotiations
• Experience in a lead or senior capacity preferred

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