RWE Clinical Project Manager (FSP)

IQVIA seeks a clinical project manager to lead real-world evidence observational studies in oncology within a dedicated team embedded at a major pharmaceutical company. The role requires end-to-end project delivery, cross-functional team leadership, and vendor management, with a minimum of 4–6 years of experience in clinical operations or RWE research and a bachelor's degree in life sciences.

Responsibilities

• Lead global cross-functional observational study teams and manage scope, timelines, and quality delivery
• Develop study documentation including project management plans and ensure SOP compliance
• Monitor study progress and financial performance; support forecasting and change control
• Manage vendor communications and activities; anticipate and mitigate operational and quality risks
• Generate project and program-level metrics and reports for senior management

Requirements

• Bachelor's degree in life sciences or related field
• 4-6 years project management or clinical operations experience in pharma, CRO, or RWE
• Demonstrated experience leading observational or real-world evidence studies
• Strong understanding of RWE study designs and clinical research regulatory requirements
• Experience with primary and secondary data collection study designs
• Cross-functional team leadership and stakeholder management skills
• Project financial management and vendor management experience

Compensation: $93,100.00 - $232,800.00 base