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What You Will Do:

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

Leading the creation, review, and optimisation of global and local informed consent forms (ICFs) in alignment with protocol, regulatory, and sponsor requirements. Advising study teams on informed consent strategy, content, and country-specific considerations, including complex or high-risk studies. Overseeing translation processes, version control, and documentation to ensure consistency and traceability across regions. Interfacing with sponsors, ethics committees, and regulatory bodies to address queries and negotiate consent wording when required. Developing and maintaining guidance, templates, and best practices to drive standardisation and efficiency. Providing training and mentorship to junior team members on informed consent principles, processes, and quality standards.

Your Profile:

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required qualifications and experience:

Bachelor's degree in a relevant scientific discipline or healthcare-related field Significant experience in clinical research, regulatory affairs, ethics, or a related function with a strong focus on informed consent. In-depth knowledge of GCP, ethical guidelines, and global regulatory expectations relating to participant information and consent. Excellent writing and editing skills, with the ability to convey complex information in clear, patient-friendly language. Strong stakeholder management and communication skills, with experience collaborating across functions and with external parties. Proven ability to manage multiple studies and priorities, with a high level of accuracy, accountability, and initiative. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply ICON is an award-winning workplace that enables you to make a difference to patients' lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you're as driven as we are, join us. You'll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. Didn't find the role you were looking for? Even if the perfect role isn't available right now, we're always excited to connect with talented individuals. 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Informed Consent Specialist II