Study Start Up Associate II - Legal Document / Contract Reviewer
About the role
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Study start up associates are integral in
ensuring that clinical research sites are prepared and have the necessary tools
and approvals needed to start the trial of investigational, new pharmaceutical
and biological products for clinical trials.
We are looking for an experience legal document reviewer. As a study start up associate at ICON
working in contracts and budgets your main role is to review and negotiate
clinical site investigator contracts and budgets. You would maintain communication
with Investigative sites, sponsors and internal personnel regarding the status
of contracts and contract-related documents, prepare and oversee preparation of
contractual documents and correspondence, and facilitate the indemnification
process between the study sponsor and the site. Further you would serve
as the internal consultant on study budgets with respect to investigator
payments, develop and update training documentation and conduct group training
as necessary, mentor and train new and junior personnel in the study start up
department, and act as consultant on the Investigator Contract and Budget
development process from origination through execution.
We are looking for associates who have existing
experience in a clinical research environment with specific experience in study
contracts review and budget negotiation or experience in a related field such
as where contract or legal document review was a primary function. A
bachelor’s degree in paralegal studies or related experience is
preferred. If you have legal document review experience, study start
up experience is desirable but is not required. We are looking for highly motivated people
with a sense of urgency and who can critically think and problem solve. You
will need to be legally authorized to work in the U.S. without
sponsorship.
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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