Clinical Research Associate

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Clinical Research Associate<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 CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This is a sponsor dedicated position looking for a candidate located in Central or Miami, FL</p><p></p><p><b>What You Will Do:</b></p><p></p><p>You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.<br><br>Key responsibilities include:</p><ul><li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li><li>Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li><li>Collaborating with investigators and site staff to facilitate smooth study conduct.</li><li>Performing data review and resolution of queries to maintain high-quality clinical data.</li><li>Contributing to the preparation and review of study documentation, including protocols and clinical study reports</li></ul><p></p><p><b>Your Profile:</b></p><p></p><p>You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.<br><br>Required qualifications and experience:</p><ul><li>Bachelor's degree in a scientific or healthcare-related field.</li><li>Minimum of 2 years of experience as a Clinical Research Associate.</li><li>In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li><li>Strong organizational and communication skills, with attention to detail.</li><li>Ability to work independently and collaboratively in a fast-paced environment.</li><li>Willingness to travel as required (approximately 60%)</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>

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