Senior CRA

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Senior Clinical Research Associate - FSP Sponsor Dedicated<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>As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p><p></p><p><b>What You Will Do:</b></p><p></p><p>You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.<br><br>Key responsibilities include:</p><ul><li><p>Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</p></li><li><p>Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.</p></li><li><p>Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.</p></li><li><p>Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.</p></li><li><p>Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.</p></li></ul><p></p><p><b>Your Profile:</b></p><p></p><p>You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.<br><br>Required qualifications and experience:</p><ul><li><p>Bachelor's degree in a relevant scientific discipline or healthcare-related field</p></li><li><p>Advanced English</p></li><li><p>Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.</p></li><li><p>Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.</p></li><li><p>Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.</p></li><li><p>Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.</p></li><li><p>Willingness to travel as required (approximately 60%)</p></li></ul><p></p><p>#LI-Remote</p><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>

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