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
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.
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!
The role * 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 need * Bachelor'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 ICON: Our success depends on the quality
of our people. That's why we've made it a priority to build a
culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them
competitive, we regularly benchmark them against our competitors.
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 - and related benefits such as life assurance - so you can
save and plan with confidence for the years ahead. But beyond the
competitive salaries and comprehensive benefits, you'll benefit
from an environment where you are encouraged to fulfil your sense
of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is
committed to providing a workplace free of discrimination and
harassment. All qualified applicants will receive equal
consideration for employment without regard to race, color,
religion, sex, sexual orientation, gender identity, national
origin, disability or protected veteran status. If, because of a
medical condition or disability, you need a reasonable
accommodation for any part of the application process, or in order
to perform the essential functions of a position, please let us
know through the form below.