Associate Director, Clinical Trial Feasibility & Site Identification - Oncology at Jobgether – United States

This position is posted by Jobgether on behalf of a partner company. We are currently looking for an Associate Director, Clinical Trial Feasibility & Site Identification - Oncology in the United States.

This role is a strategic and highly analytical position focused on driving data-informed planning and execution for oncology clinical trials. The Associate Director will provide expert guidance on site selection, feasibility assessments, and enrollment strategies across the clinical portfolio. By integrating historical, predictive, and real-world data, this position informs protocol design, optimizes site activation, and supports efficient trial execution. The role works closely with cross-functional teams, including Clinical Operations, Clinical Development, and Medical Affairs, to ensure feasibility insights are embedded throughout study planning. It also involves oversight of vendor and CRO partnerships to ensure high-quality deliverables. This position is remote, offering collaboration across teams nationwide, with opportunities to influence trial design and operational excellence at a global level.

• Serve as a subject matter expert in oncology clinical trial feasibility and site intelligence to guide operational planning and protocol design.
• Develop study scenarios and placement strategies by analyzing country and site data, enrollment projections, and site activation timelines.
• Partner with cross-functional teams to integrate feasibility insights into clinical study planning and execution.
• Lead site identification and selection, ensuring alignment with protocol requirements and operational priorities.
• Provide functional oversight of vendors and CROs supporting feasibility, including performance management and budget oversight.
• Utilize historical data, real-world evidence, and emerging technologies to optimize trial design, reduce operational risk, and improve efficiency.
• Contribute to defining KPIs and operational metrics for site performance, recommending improvements based on data-driven insights.

Requirements:

• Bachelor’s degree in life sciences, healthcare, or a related field; advanced degree preferred.
• 8–10 years of clinical research experience, with at least 5 years in clinical trial feasibility, site intelligence, or related functions.
• Demonstrated expertise in global feasibility assessment, enrollment modeling, and data-driven site selection.
• Experience leveraging real-world data, digital technologies, and AI/ML tools to inform study planning.
• Proven ability to influence cross-functional decision-making through insights and analytics.
• Strong understanding of vendor and CRO evaluation, collaboration, and oversight.
• Excellent organizational, communication, and teamwork skills with the ability to build effective partnerships across internal and external stakeholders.
• Ability to contribute to inspection readiness, continuous process improvement, and adoption of innovative tools to optimize operations.

Benefits:

• Competitive base salary range: $164,000 – $246,000, with individual compensation aligned to experience, qualifications, and contributions.
• Potential eligibility for discretionary annual cash bonuses and long-term equity incentive plans.
• Comprehensive medical, dental, and vision insurance coverage.
• 401(k) retirement savings plan with employer match.
• Flexible paid vacation and remote work options.
• Opportunities to contribute to high-impact oncology clinical trials and shape operational excellence.