.Senior Site Activation LeadLocations: Mexico, Mexico City; Brazil, Sao Paulo;Colombia, Bogota; Peru, LimaTime Type: Full timePosted on: Posted 4 Days AgoJob Requisition ID: JR123736Sr. SAL (Home based)ICON 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 fulfill 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.The role:The Senior Site Activation Lead (Sr. SAL) is accountable for driving and accelerating the activation of investigative sites in line with, or ahead of, the study's contractual timelines, budgeted resources, quality output, and sponsor expectations. The Sr. SAL is accountable for the overall coordination, implementation, and completion of site activation activities for large global or complex projects of work in line with ICON/sponsor SOPs as appropriate.Some responsibilities:Primary study start-up point of contact for designated complex and/or global projects.Accountable for developing successful working relations with sponsors, as evidenced by high sponsor satisfaction scores in SSU, to ensure repeat business.Defines project scope, including resource requirements and deliverables, from a study start-up perspective.Accountable for writing and maintaining the site activation plans to deliver to contract and target, ensuring sites are progressed after identification to subject dosing without delay.Accountable for the risk management and mitigation strategies within site activation to ensure timely delivery.Working cross-functionally to ensure that the sites and countries optimize accelerated delivery of the project.Ensure stringent oversight of project in terms of timely and quality delivery of key milestones and that the impact of missed deliverables is clearly and timely communicated to all key stakeholders.What you need:Bachelor's degreeExcellent English skills.Experience in oversight of study deliverables, ideally with proven experience in the oversight of site activation project management and staff oversight; experience working in aglobal/multi-regional environment preferred.Minimum 5 years' experience within clinical research with experience in SSU and Site Activation.Due to the nature of this position, it may be required for the employee to travel, including air travel.Dependent on the employee's location, the employee may be Home based (LATAM)