Study Start Up Associate II - Informed consent forms - Colombia and Mexico - Homebased

• Your main role is to review Informed Consent Forms and negotiate language as needed
• You will 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.
• You will assist in the drafting of ICF country templates for the United States and Canada, which are then distributed to study sites to make edits depending on their local IRB requirements and SOPs

• Bachelor’s degree in life sciences or similar
• Advanced English level
• Associates who have a background in clinical research at a CRO, Pharmaceutical company, study site, or who have worked at an IRB
• Experience performing ICF review as an essential function of the job