Senior Site Activation Lead

Detalles de la oferta

Senior Site Activation LeadApply locations: Mexico, Mexico City; Bulgaria, Sofia; Poland, Warsaw
Time type: Full time
Posted on: Posted 5 Days Ago
Job requisition id: JR126783 Sr. 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.
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.
The RolePrimary 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 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 projects 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 NeedBachelor's Degree preferably in life sciences.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.Benefits of Working in ICONWe offer very competitive salary packages.
Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans.
Our benefits examples include:
Various annual leave entitlements.A range of health insurance offerings to suit you and your family's needs.Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.Global Employee Assistance Programme, offering 24-hour access to a global network of specialized professionals.Life assurance.Flexible country-specific optional benefits.At ICON, diversity, inclusion & belonging are fundamental to our culture and values.
We're dedicated to providing an inclusive and accessible environment for all candidates.
If you need a reasonable accommodation for any part of the application process, please let us know.
Interested in the role, but unsure if you meet all of the requirements?
We encourage you to apply regardless.

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Salario Nominal: A convenir

Fuente: Jobleads

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