Study Start Up Associate II - Informed Consent Form Reviewer

ICF (Informed Consent Form) Reviewer -- Study Start Up Associate II

Europe / Australia / New Zealand

We are looking for someone with Informed Consent Form review/creation experience (ICF Reviewer) to join our Informed consent team.

As a Study Start Up Associate at ICON working as an Informed Consent Form Reviewer/Creator your main role is to create/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.