<?xml version="1.0" encoding="UTF-8"?>
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    <job>
      <externalid>bafcf0aa-f62</externalid>
      <title>Single Sponsor Clinical Project Director (Program Manager) - 3 days in the Dublin office</title>
      <description><![CDATA[<p>We are seeking a Single Sponsor Clinical Project Director (Program Manager) to join our Clinical Solutions team in Dublin. As a Clinical Project Director, you will play a leadership role in managing a team of direct reports and indirect reports, and will be responsible for overseeing the successful execution of studies and/or multiple studies within a program or multiple programs.</p>
<p><strong>Responsibilities</strong></p>
<ul>
<li>Manage a team of direct reports and indirect reports, and lead ongoing training and coaching of team members</li>
<li>Provide input into strategic and operational short- and long-range therapeutic area / functional area plans</li>
<li>Champion Syneos Health&#39;s Values and Leadership Commitments</li>
<li>Oversee the successful execution of studies and/or multiple studies within a program or multiple programs, including financial responsibility</li>
<li>Lead or oversee study teams related to assigned studies</li>
<li>Proactively manage vendor engagement and stakeholder relationships at the study-level</li>
<li>Develop operational strategies for studies to optimize execution</li>
<li>Act as a manager of managers and individual contributors with a People First approach</li>
<li>Manage resources for assigned studies, including assessing resource needs and deploying resources effectively</li>
<li>Participate in Clinical Operations and/or cross-functional change initiatives</li>
<li>Lead or engage in Clinical Operations-specific change initiatives</li>
<li>May have business process owner (BPO) responsibilities and/or serve as a subject matter expert for Clinical Operations processes</li>
<li>Encourage an innovative mindset by championing new ideas and initiatives</li>
<li>Ensure team&#39;s work complies with established practices, policies, and processes, and regulatory requirements</li>
</ul>
<p><strong>Requirements</strong></p>
<ul>
<li>BA / BS / RN with end-to-end program management experience, and a solid background in Clinical Trial Management or Clinical Project Management</li>
<li>Operating at a high level in a cross-functional study management or related leadership experience in CRO or Pharma, including multiple years&#39; experience leading and managing study management or project teams</li>
</ul>
<p style="margin-top:24px;font-size:13px;color:#666;">Job Data by <a href="https://yubhub.co">YubHub</a>.</p>]]></description>
      <jobtype>full-time</jobtype>
      <experiencelevel>senior</experiencelevel>
      <workarrangement>hybrid</workarrangement>
      <salaryrange></salaryrange>
      <skills>Clinical Trial Management, Clinical Project Management, Leadership, Team Management, Strategic Planning</skills>
      <benefits></benefits>
      <licences></licences>
      <category>Healthcare</category>
      <industry>Healthcare</industry>
      <employername>Syneos Health</employername>
      <employerlogo>https://logos.yubhub.co/syneoshealth.com.png</employerlogo>
      <employerdescription>Syneos Health is a leading fully-integrated life sciences services organization that partners with innovators across the drug development and commercialization continuum.</employerdescription>
      <employerwebsite>http://www.syneoshealth.com</employerwebsite>
      <compensationcurrency></compensationcurrency>
      <compensationmin></compensationmin>
      <compensationmax></compensationmax>
      <compensationinterval></compensationinterval>
      <applyto>https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/IRL-Client/Single-Sponsor-Associate-Clinical-Project-Director--Program-Manager----3-days-in-the-Dublin-office_25111867</applyto>
      <location>IRL-Client</location>
      <city>IRL-Client</city>
      <state></state>
      <postalcode></postalcode>
      <country>IE</country>
      <postedate>2026-10-14</postedate>
      <visasponsorship>unknown</visasponsorship>
      <visasponsorshiptext><![CDATA[]]></visasponsorshiptext>
      <workauthorisation>unknown</workauthorisation>
    </job>
  </jobs>
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