ICON PLC

Senior Site Activation Lead (BB-03351)

Found in: Neuvoo IN

Description:
As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry! Are you one of them? At ICON, we have an incredible opportunity for a Senior Site Activation Lead to join the team. The Role 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 organisation Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation 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 is our vision. We are driven by it. And we need talented people who share it. If you are as driven as we are, join us. You will 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. As a Senior Site Activation Lead at ICON, you are accountable for driving and accelerating the activation of investigator sites. Additionally you will be accountable for the implementation and completion of site activation activities for global, complex projects. As a Senior Site Activation Lead you will work cross functionally throughout ICON and with ICON sponsors, ensuring a positive customer experience throughout the relationship! Primary SSU point of contact for designated global projects and programs Accountable for developing successful sponsor relationships, proven through consistently high sponsor satisfaction scores in SSU, contributing to the retention and repeat business. Working cross-functionally to ensure sites and countries optimize accelerated delivery of the project Risk management and mitigation strategies within site activation to ensure timely delivery Ensure stringent oversight of project in terms of timely and quality delivery of key landmarks Accountable for management of sponsor expectations and ensuring compliance with ICON / Sponsor critical metrics; SOPs; and quality standards. Responsible for the study start up budget, including resources; timelines; rates and margins. What you will need Bachelor's Degree preferably in life sciences 5 years in depth proven experience within clinical research, specifically in the clinical studies regulatory environment. Excellent Leadership skills, developed with a collaborative approach to driving performance and success Experience in successful management and delivery of study deliverables, ideally with proven experience in the oversight of project management and staff in a multi-country / global environment. Cross functional leadership and influencing skills Strong planning and organization skills within a time pressured environment. Excellent written and verbal communication, fluent in English

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