Informed Consent Specialist II/Sr

Informed Consent Specialist I - Homebased - Colombia and Chile<br><p>ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.</p><br><p>As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.</p><br><div>As an Informed Consent Specialist II at ICON, you will support the development, review, and management of informed consent documents to ensure they are clear, compliant, and patient-focused.</div><div><div><div><div><div><div><div><div><div><p></p><p><b>What You Will Do:</b></p><p></p><p>You will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency.<br><br>Key responsibilities include:</p><ul><li><p>Responsible for the preparation and review of informed consent forms (ICFs) in accordance with protocols, regulations, and sponsor requirements.</p></li><li><p>Coordinating the collection and tracking of ethics committee and regulatory approvals related to informed consent documents.</p></li><li><p>Supporting the management of consent templates, translations, and version control across countries and sites.</p></li><li><p>Liaising with internal teams to address basic questions and clarifications regarding consent language and requirements.</p></li><li><p>Ensuring accurate filing and documentation of informed consent materials to maintain audit and inspection readiness.</p></li><li><p>Contributing to process improvements and standardization efforts within the informed consent function.</p></li></ul><p></p><p><b>Your Profile:</b></p><p></p><p>You will bring relevant clinical research experience, along with the following qualifications and skills.<br><br>Required qualifications and experience:</p><ul><li><p>Bachelor's degree in life sciences, healthcare, legal studies, or a related field, or equivalent experience.</p></li><li><p>Experience in clinical research, regulatory affairs, ethics submissions, or document management.</p></li><li><p>Broad understanding of informed consent principles, GCP, and ethical requirements.</p></li><li><p>Strong attention to detail and organisational skills, with the ability to manage multiple document versions and timelines.</p></li><li><p>Clear written and verbal communication skills, with a patient-centric approach to document content.</p></li><li><p>Proficiency with MS Office and comfort working with document management systems and trackers.</p></li></ul></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><div><p></p><p>#LI-FB2</p><p>#LI-Homebased</p></div></div></div></div></div></div></div></div><br><p>Employment with ICON is contingent upon having the legal right to work in the country where the role is based.</p><br><p><b>Rewards & Benefits</b></p><p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p><br><p>Benefits may include:</p><ul><li>Competitive base salary and performance related incentives</li><li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li><li>Retirement and pension plans</li><li>Life assurance and disability coverage</li><li>Employee assistance programmes and wellbeing resources</li><li>Learning and development opportunities through structured training and career pathways</li></ul><br><p>Benefits may vary depending on role and location.</p><br><p>Visit our <a href="https://careers.iconplc.com/benefits" target="_blank" rel="noopener noreferrer">careers site</a> to read more about the benefits ICON offers.</p><br><p><b>Inclusion and Accessibility</b></p><p>ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.</p><br><p>If you require reasonable accommodations during the recruitment process, please let us know or submit a request <a href="https://careers.iconplc.com/reasonable-accommodations" target="_blank" rel="noopener noreferrer"><span style="color:#0875e1"><b><u>here</u></b></span></a>.</p><p style="text-align:inherit"></p><p style="text-align:left"><span>Are you a current ICON Employee? Please click </span><a href="https://wd3.myworkday.com/icon/d/task/1422$1235.htmld" target="_blank" rel="noopener noreferrer">here</a><span> to apply</span></p>