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      <externalid>24fbd086-37d</externalid>
      <title>CRA I</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 CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.</p>
<p><strong>Responsibilities</strong></p>
<p>Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders. Key responsibilities include:</p>
<ul>
<li>Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation</li>
<li>Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.</li>
<li>Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.</li>
<li>Ensure patient safety by ensuring compliance with ICON&#39;s procedures, protocols, and regulatory requirements.</li>
</ul>
<p><strong>Your Profile</strong></p>
<p>You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:</p>
<ul>
<li>University degree in medicine, science, or equivalent</li>
<li>Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data</li>
<li>Excellent written and verbal communication in English</li>
<li>Good social skills enabling you to deal with queries in a timely manner</li>
<li>Willingness to travel as required (approximately 60%)</li>
</ul>
<p><strong>Rewards &amp; Benefits</strong></p>
<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>
<p>Benefits may include:</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></experiencelevel>
      <workarrangement></workarrangement>
      <salaryrange></salaryrange>
      <skills>ICH-GCP guidelines, medical data analysis, 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/Regional-Guatemala-PRA/CRA-I_JR163188</applyto>
      <location>Regional Guatemala (PRA</location>
      <city>Regional Guatemala (PRA</city>
      <state></state>
      <postalcode></postalcode>
      <country>GT</country>
      <postedate>2026-10-27</postedate>
      <visasponsorship>unknown</visasponsorship>
      <visasponsorshiptext><![CDATA[]]></visasponsorshiptext>
      <workauthorisation>required</workauthorisation>
    </job>
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