Site Activation Leader (West Coast Remote)

Site Activation Leader (West Coast Remote) at Parexel in Boise, Idaho, United States Job Description Site Activation Leader We are seeking a highly driven Site Activation Leader to join our Site Activation Center of Excellence. In this role, you will lead the planning, execution, and oversight of site activation across clinical trials-ensuring studies are initiated on time, within scope, and to the highest quality standards. You will play a critical role in accelerating clinical research by driving efficient site start-up activities from feasibility through activation across multiple studies and therapeutic areas. We are focusing on hiring an individual on the west coast for this position.

What You'll Do:

Site Activation Leadership & Strategy + Lead site activation strategy and execution for assigned clinical studies + Oversee all start-up milestones from feasibility through site activation + Develop and manage study critical path plans, including regulatory and operational activities + Identify risks, proactively mitigate delays, and ensure delivery timelines are met + Drive cross-functional problem solving to resolve complex activation challenges Team & Stakeholder Leadership + Guide and mentor site activation team members + Act as a key liaison between project management, start-up teams, and stakeholders + Communicate activation progress, risks, and solutions to internal teams and leadership + Collaborate with clinical operations to align with study objectives Client Engagement & Business Support + Serve as the Study Start-Up (SSU) subject matter expert for assigned clients + Provide strategic guidance and best practices for study initiation + Support proposal development and bid defense activities Process Improvement & Quality + Implement standardized processes and best practices across studies + Analyze metrics to drive continuous improvement and operational efficiency + Ensure compliance with regulatory requirements, SOPs, and GCP + Contribute to process, template, and documentation development Systems & Reporting + Leverage CTMS, EDC, IXRS, and TMF systems to optimize workflows + Ensure data integrity and accurate documentation across studies + Develop reports, metrics, and insights for leadership decision-making

What You Bring:

Experience + 4-7 years in clinical research operations, including site activation leadership + Proven experience managing site activation activities and teams + Strong understanding of clinical trial start-up processes and timelines + Experience working wi

Job Posting:

JC291631717

Posted On:

May 10, 2026

Updated On:

May 10, 2026