Informed Consent Specialist II

Informed Consent Specialist II
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
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.
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.
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.
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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

Skills
GCP, Clinical Research, Regulatory Affairs, Documentation