Informed Consent Specialist II

Informed Consent Specialist II<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><p>As an Informed Consent Specialist II at ICON, you will take a lead role in the development, review, and oversight of informed consent documents for complex, global clinical trials.</p><p></p><p><b>What You Will Do:</b></p><p>Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.<br><br>Key responsibilities include:</p><ul><li><p>Leading the creation, review, and optimization of global and local informed consent forms (ICFs) in alignment with protocol, regulatory, and sponsor requirements.</p></li><li><p>Advising study teams on informed consent strategy, content, and country-specific considerations, including complex or high-risk studies.</p></li><li><p>Overseeing translation processes, version control, and documentation to ensure consistency and traceability across regions.</p></li><li><p>Interfacing with sponsors, ethics committees, and regulatory bodies to address queries and negotiate consent wording when required.</p></li><li><p>Developing and maintaining guidance, templates, and best practices to drive standardization and efficiency.</p></li><li><p>Providing training and mentorship to junior team members on informed consent principles, processes, and quality standards.</p></li></ul><p></p><p><b>Your Profile:</b></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 a relevant scientific discipline or healthcare-related field</p></li><li><p>Significant experience in clinical research, regulatory affairs, ethics, or a related function with a strong focus on informed consent.</p></li><li><p>In-depth knowledge of GCP, ethical guidelines, and global regulatory expectations relating to participant information and consent.</p></li><li><p>Excellent writing and editing skills, with the ability to convey complex information in clear, patient-friendly language.</p></li><li><p>Strong stakeholder management and communication skills, with experience collaborating across functions and with external parties.</p></li><li><p>Proven ability to manage multiple studies and priorities, with a high level of accuracy, accountability, and initiative.</p></li><li><p></p></li></ul><p>#LI-JJ1</p><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>

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