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    <job>
      <externalid>14ab3b89-895</externalid>
      <title>Site Specialist II</title>
      <description><![CDATA[<p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p>
<p>As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contribute to efficient study start-up and maintenance.</p>
<p><strong>Responsibilities</strong></p>
<ul>
<li>Coordinating site-level document collection, review, and maintenance, ensuring accuracy and compliance for assigned sites or studies.</li>
<li>Acting as an operational liaison for site staff on documentation, systems, and process-related questions.</li>
<li>Deliver regulatory submissions in accordance with contractual timelines, budget, and quality standards.</li>
<li>Contribute to strategic planning of submissions to Regulatory Authorities (RA), Central Ethics Committees (CEC), and other applicable bodies.</li>
<li>Maintaining up-to-date site status, metrics, and key milestones in clinical trial management tools.</li>
<li>Supporting planning and logistics for site meetings, investigator meetings, and monitoring visits.</li>
<li>Identifying opportunities to streamline site workflows and contributing to process improvement initiatives.</li>
<li>Providing guidance to Site Specialist I or junior colleagues, sharing best practices and supporting their development.</li>
</ul>
<p><strong>Your Profile</strong></p>
<ul>
<li>Bachelor&#39;s degree in life sciences, healthcare, business, or a related field, or equivalent clinical research experience.</li>
<li>Relevant experience in site support, clinical administration, or similar roles within CRO, pharma, or healthcare.</li>
<li>Experienced with a minimum of 3 years’ relevant regulatory experience in clinical research.</li>
<li>Fluent in Swedish and English.</li>
<li>Good understanding of clinical trial processes, GCP, and site documentation requirements.</li>
<li>Strong organisational and problem-solving skills, with the ability to manage multiple sites and priorities.</li>
<li>Excellent communication and interpersonal skills, with a proactive, service-focused mindset.</li>
<li>Comfort working independently while collaborating effectively with cross-functional teams.</li>
</ul>
<p><strong>Rewards &amp; Benefits</strong></p>
<ul>
<li>Competitive base salary and performance related incentives</li>
<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>
<li>Retirement and pension plans</li>
<li>Life assurance and disability coverage</li>
<li>Employee assistance programmes and wellbeing resources</li>
<li>Learning and development opportunities through structured training and career pathways</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></workarrangement>
      <salaryrange></salaryrange>
      <skills>life sciences, healthcare, business, clinical research, regulatory experience, GCP, site documentation, organisational skills, problem-solving skills, communication skills, interpersonal skills, Swedish, English</skills>
      <benefits>pension, health_insurance, dental</benefits>
      <licences></licences>
      <category>Healthcare</category>
      <industry>Healthcare</industry>
      <employername>ICON</employername>
      <employerlogo>https://logos.yubhub.co/icon.com.png</employerlogo>
      <employerdescription>ICON is a global healthcare intelligence and clinical research organisation.</employerdescription>
      <employerwebsite>https://icon.com</employerwebsite>
      <compensationcurrency></compensationcurrency>
      <compensationmin></compensationmin>
      <compensationmax></compensationmax>
      <compensationinterval></compensationinterval>
      <applyto>https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Sweden-Lund/Site-Specialist-II_JR159903</applyto>
      <location>Lund, Sweden</location>
      <city>Lund</city>
      <state>Sweden</state>
      <postalcode></postalcode>
      <country>SE</country>
      <postedate>2026-10-26</postedate>
      <visasponsorship>unknown</visasponsorship>
      <visasponsorshiptext><![CDATA[]]></visasponsorshiptext>
      <workauthorisation>required</workauthorisation>
    </job>
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