Manager

• Develops and builds the US budget, site budget & language templates for Pharma & Vaccine studies
• Provides expert guidance to develop detailed specifications and negotiate content of clinical trial agreements
• Participates in creating and delivering solutions for simplifying work practices to increase productivity
• Perform due diligence checks which includes but is not limited to Fair Market Value and review of site justifications
• Escalate delays, impact to timelines, or risks that limit the ability to deliver a fully executed CTA within the timelines specified
• Timely and accurate updating of all departmental databases and trackers
• Train and support additional team members as required

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