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Study Start Up Associate II ( Informed Consent Forms )

Study Start Up Associate II (Informed Consent Forms) o you have experience reviewing and negotiating language in Informed Consent Forms?  If so, we have a career opportunity in the exciting world of drug discovery for you.   We are looking for someone with Informed Consent Form review/creation experience (ICF Reviewer) to join our Centralized Informed consent team.    As a Study Start Up Associate at ICON working as an Informed Consent Form Reviewer/Creator your main role is to review country and site level Informed Consent Forms and negotiate language as needed.  You will also be involved in drafting of Global Master ICFs, which are then distributed to study teams to make edits depending on their local country requirements and SOPs. You will then review and negotiate these changes and potentially liaise with other stakeholders like the sponsor, legal, or the clinical team to ensure that changes to the ICF are acceptable.   We are looking for associates who have a background in clinical research at a CRO, Pharmaceutical company, study site, or who have worked at an IEC/IRB. Your experience should include performing ICF related tasks as an essential function or part of the job.    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. Reference: 054107  
Salary Range: NA
Minimum Qualification
Not Specified years

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