Informed Consent Specialist II
- Sofia, Prague, Riga, Vilnius, Warsaw, Johannesburg, Madrid, Bratislava
- Study Start Up
- ICON Full Service & Corporate Support
- Remote or Office
Talent Acquisition Business Partner
- Full Service Division
About the role
Informed Consent Specialist II
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
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 optimization 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 standardization 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.
#LI-JJ1
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
Explore more about ICON
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
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