Site Activation Lead
About the role
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Do you have experience in Study Start Up initiatives and are
now looking to further develop, implement and execute a Study Start Up Strategy?
As a Site Activation Lead you would advance clinical trial
start-up activities by understanding the clients’ objectives and assist them in
the development of the plan for country and site distribution. The
successful candidate will show capability in the areas of clinical trial operations,
meeting regulatory and ICON guidelines, and displaying project management
skills to optimize performance and collaboration to ensure successful study
outcomes. You will need Global Study Start up experience leading sponsor
initiatives such as kick-off meetings, bid defenses, project update and status
calls, and other communications. We ask that you have a Bachelor’s
degree, project and client interaction skills, and experience leading study
start up activities globally in a clinical research environment.
Our SAL is selected to lead clinical trial start-up
activities by understanding the clients’ objectives and assist in the
development of the plan for country and site distribution. You will show
capability in the areas of Clinical Trial operations, meeting regulatory and
ICON guidelines and displaying project management skills to optimize
performance and collaboration to ensure successful study outcomes.
To succeed you will need a Bachelor’s Degree preferably in
life sciences with great project management skill set and understanding of
regulatory and submission processes in many different countries along with a
minimum of five years of experience in a clinical research environment
(preferable focusing on Start Up Activity).
We prefer Global Study Start Up experience as well as leading sponsor
meetings and communications. This is a
home-based role and can be located in any U.S. location.
We are a company of 13,500 employees in forty countries
globally. We differentiate ourselves by developing innovative solutions
to bring life-saving drugs to market faster and in a more cost-effective way to
foster better patient outcomes. We are a
top five clinical research organization with solid earnings and growth
potential. Our belief in excellence is
our core value in all that we do for our sponsor partners and the patients that
we serve. As a company we strive to exceed our customers’ expectations in
drug development solutions.
Other than working with a great team of smart and energetic
people, we also offer a very competitive salary and benefits package that
includes an excellent retirement plan, health coverage, paid time off, income
protection insurance programs, and staff recognition schemes. We care
about our people, since they are the key to our success. We provide an open and
friendly work environment where we empower people and provide them with
opportunities to develop their long term career. Caring for patients while enjoying what we do
and delivering great results is something we can achieve if we know we can
count on each other and have a clear vision of where we want to go.
ICON is an equal opportunity employer –
Minorities/Females/Disabled/Veterans and committed to providing a workplace
free of any discrimination or harassment.
Application process
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Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
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