Regional Director, Sites

Iterative Scopes Inc.

  • Cambridge, MA
  • 29 days ago
    Want to know if you’re a fit?
    Upload your resume and let our AI show you.

    Skills

    • Change Managementunmatched
    • Clinical Researchunmatched
    • Clinical Trialunmatched
    • Coachingunmatched
    • Communication Skillsunmatched
    • Conferencesunmatched
    • Continuous Improvementunmatched
    • Corrective Actionunmatched
    • Data Qualityunmatched
    • Dental Insuranceunmatched
    • Electronic Data Capture (EDC)unmatched
    • Follow Throughunmatched
    • Gastroenterologyunmatched
    • Hepatologyunmatched
    • Identify Issuesunmatched
    • Management Strategyunmatched
    • Operational Strategyunmatched
    • People Managementunmatched
    • Performance Analysisunmatched
    • Performance Metricsunmatched
    • Presentation/Verbal Skillsunmatched
    • Problem Solving Skillsunmatched
    • Process Improvementunmatched
    • Profit & Lossunmatched
    • Project/Program Managementunmatched
    • Regulatory Requirementsunmatched
    • Resource Managementunmatched
    • Strategic Planningunmatched
    • Team Buildingunmatched
    • Trend Analysisunmatched
    • Vision Planunmatched
    • Willing to Travelunmatched
    • Writing Skillsunmatched

    Description

    About the Role

    The Regional Director is responsible for owning and optimizing site-level performance across a portfolio of GI-focused clinical research sites. This role ensures operational excellence by aligning teams around key performance goals, elevating site capabilities, and maintaining consistency in trial execution. As a strategic operations leader, the Regional Director plays a central role in connecting site level performance with broader business objectives.

    Responsibilities

    • Manages staff across multiple sites, ensuring execution is aligned with protocol, regulatory requirements, and IH standards.
    • Owns overall performance of assigned sites, including enrollment, data quality, compliance, and team culture.
    • Ensures sites are set up for success (i.e. staffed appropriately and equipped with the appropriate equipment and training) and makes recommendations to allocate resources based on business needs.
    • Builds strong relationships and collaborates with PIs to align their engagement with study goals and operational strategy.
    • Influences study portfolio, optimizing for profitability and value to patients.
    • Identifies and manages issues, concerns and problems related to site performance.
    • Leads and develops CRCs, and other site-based research staff through clear expectations, performance coaching, and team development.
    • Serves as a visible, hands-on people manager who builds high-performing, accountable teams.
    • Identifies levers to drive site level KPIs through monitoring KPIs and performance trends, escalating to appropriate parties.
    • Implements corrective actions or process improvements as needed.
    • Serves as the primary operational liaison between site staff and central functions.
    • Drives a culture of ownership, collaboration, and continuous improvement across all assigned sites.

    What We're Looking For

    Required Qualifications

    • Knowledgeable about the critical elements for success in clinical trials: Ability to review protocols, programs, and assess the success of a project.
    • Ability to influence change management and model flexibility
    • Problem-Solving Skills: Ability to identify problems, develop and implement solutions.
    • Strategic Planning: Ability to plan for short, medium and long term success and make recommendations for growth
    • Ability to use data as a tool, identify trends, and draw conclusions.
    • Project Management: Demonstrated ability to successfully manage people/projects.
    • Proactive problem-solving abilities and follow-through.
    • Practices professionalism and integrity in all actions.
    • Communication Skills: Excellent written and verbal communication skills.
    • Working knowledge of CTMS, eDC and other core research systems.
    • Ability to travel: Up to 30% travel to provide operational oversight, hold team meetings, and attend other professional meetings/conferences as needed.

    Preferred Qualifications

    • Experience in managing a large site network and demonstrated success in achieving targets and optimizing operations.
    • Experience with gastroenterology and/or hepatology studies.

    What We Offer

    • Medical, dental, and vision insurance
    • Life and disability insurance
    • Parental leave
    • Stock options
    • Flexible work hours
    • Unlimited paid time off

    Numbers & Facts

    LocationCambridge, MA

    Similar Jobs

    See more jobs