Home Based- CDMX<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 Study Start Up Associate I at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments and therapies.</p><br><p><b>What You Will Do:</b></p><p>Your role will involve delivering site start-up and activation work to a high standard, working closely with your team and stakeholders.<br><br>Key responsibilities include:</p><ul><li>Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.</li><li>Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.</li><li>Maintaining accurate and up-to-date records of regulatory submissions and approvals.</li><li>Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures.</li><li>Participating in study start-up meetings and providing input on regulatory requirements and timelines.</li></ul><br><p><b>Your Profile:</b></p><p>You will bring relevant site start-up and activation experience, along with the following qualifications and skills.<br><br>Required qualifications and experience:</p><ul><li>Bachelor's degree in life sciences or a related field.</li><li>Previous experience in clinical research or regulatory affairs preferred, but Nt required.</li><li>Strong attention to detail and organizational skills.</li><li>Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.</li><li>Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.</li><li>Willingness to travel as required (approximately 5%)</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>