.Study Start Up Associate I - Site Activation Associate I - Mexico - RemoteICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.The Role:Study Start Up Associate I (Site Activation Associate I)Summary:Participate on clinical trial Start Up activities by understanding the clinical site activation requirements and assist the sites in their progress, ensuring that site activation is executed according to plans.Responsibilities:Oversees day to day execution and site progress for all aspects and tasks related to site activation for the assigned projects and sites.Assist and engage with sites to ensure that site staff team members are progressing throughout site activation in accordance with the site activation plans and in compliance with ICON/client KPIs, ICON/client SOPs.Support internal tools set up, maintenance, and timely updates and ensure site adoption of ICON tools. Contribute to effective site activation process and timelines.Participate in internal study reviews with study teams to contribute to risk identification and action planning.To be successful in the role, you will have:Bachelor's Degree preferably in life sciencesMinimum of 1 to +2 years of experience in Clinical Research environment (Experience as CTA, Clinical Associate, Senior CTA, IHCRA, CRA I is a plus)Project management skill setExcellent English written and verbal communicationAbility to work to tight deadlinesBenefits of Working in ICON:Our success depends on the knowledge, capabilities and quality of our people. That is why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development