Clinical Research

• Act as the functional lead responsible for site identification activities across all study types and phases
• Develop and implement protocol-specific site identification strategies
• Design protocol-specific site questionnaires and analyze investigator responses
• Lead locally assigned teams to deliver prequalified sites, including training, survey launch, and issue escalation
• Deliver revised enrollment scenarios and final lists of prequalified sites
• Prepare slide decks and integrated reports presenting site selection outcomes, methodology, results, and recommendations
• Revise protocol feasibility assessments and country selection analyses using post-award data
• Manage country clinical operations surveys and compile data into country selection analyses, scenario modeling, and site identification strategies
• Contribute to optimized operational strategies for patient recruitment and enrollment scenarios
• Present and defend country/site selection strategies and enrollment models in internal and Sponsor meetings
• Act as Project Leader on stand-alone feasibility studies under management supervision, including Sponsor liaison, project initiation, resource planning, implementation, milestone tracking, progress reporting, and communication management
• Attend Bid Defense and Sponsor Kick-Off Meetings and present feasibility/prequalification services
• Serve as Subject Matter Expert for an identified feasibility system, tool, or process

Explore Clinical Feasibility Leader at Parexel. Review requirements and application details.