Clinical Research

• Responsible for executing Tempus’s observational trials in compliance with quality standards (ICH/GCP, Global Regulations, and Tempus policies and procedures)
• Act as primary point of contact for clients.
• Anticipate client needs and proactively resolve issues as necessary
• Lead cross-functional teams and third parties/vendors to ensure effective teamwork and communication
• Manage project deliverables including timeline, quality, scope, and cost
• Maintain study management system(s)
• Develop and maintain project plans
• Primary contact for assigned sites and build positive relationships with investigators and site staff
• Complete monitoring visits and/or oversee Clinical Research Associates, as applicable
• Manage participant recruitment, sample reconciliation, data entry to safe-guard project endpoints
• Responsible for the completeness and quality of the Trial Master File
• Provide temporary coverage/back-up for additional observational studies as required
• May involve overnight travel

Clinical Study Manager

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