Clinical Trial Liaison<br><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><br><p>As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.</p><br><p><u>Clinical Investigator Management</u> </p><ul><li>Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout </li><li>Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements </li><li>Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas </li><li>Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives </li><li>Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc </li><li>Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct </li></ul><p><u>Clinical Trial Management</u> </p><ul><li>Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery </li><li>Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones </li><li>Drive inspection readiness as a continuous discipline across sites </li><li>Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality </li><li>Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization </li><li>Provide oversight and quality assurance for vendor monitoring, escalating risks proactively </li><li>Where applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations </li><li><u>Business Management and Engagement</u> </li><li>Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize client trials </li><li>Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner </li><li>Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity </li><li>Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution </li><li>Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel </li><li>Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer </li><li>Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships </li></ul><p><br><b>Your profile </b></p><ul><li>Bachelor’s degree or equivalent; strong preference for scientific, clinical, or health-related fields </li><li>Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites  </li><li>Open to up to 60-80% travel during peak times (travel will vary)</li><li>Oncology experience required (lung cancer experience preferred)</li><li>Location US Southeast</li></ul><br><p>Employment with ICON is contingent upon having the legal right to work in the country where the role is based.</p><br><p><b>Rewards & Benefits</b></p><p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p><br><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><br><p>Benefits may vary depending on role and location.</p><br><p>Visit our <a href="https://careers.iconplc.com/benefits" target="_blank" rel="noopener noreferrer">careers site</a> to read more about the benefits ICON offers.</p><br><p><b>Inclusion and Accessibility</b></p><p>ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.</p><br><p>If you require reasonable accommodations during the recruitment process, please let us know or submit a request <a href="https://careers.iconplc.com/reasonable-accommodations" target="_blank" rel="noopener noreferrer"><span style="color:#0875e1"><b><u>here</u></b></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Are you a current ICON Employee? Please click </span><a href="https://wd3.myworkday.com/icon/d/task/1422$1235.htmld" target="_blank" rel="noopener noreferrer">here</a><span> to apply</span></p>