Clinical Trial Subject Matter Expert (CT SME)

Clinical Trial Subject Matter Expert (CT SME)

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.

What you will be doing

• Uses clinical research experience, accrued from previous clinical research roles, to assist colleagues in the production of accurate and engaging components for our stakeholders.

• Works actively, independently or with the team (depending on the task), to create the high quality digital solutions in line with the sponsor's needs and expectations, and within sponsor delivery timelines.

• Advises and supports the production team (Instructional Designer, Graphic Designer, Product Testing Analysts) on clinical trial related matters, across therapeutic areas.

• Ensures technical accuracy of the products/solutions at each stage of the product development, while ensuring the clinical content adds maximum value for end users (Sponsors, Site Staff, Investigators, and Patients).

• Conducts comprehensive review of study documentation provided by the sponsor

• Attends sponsor meetings and assists Project Manager (PM) as required to support product development

• Communicates/escalates protocol-related queries to the Project Manager (PM)/In Team Lead (ITL).

• Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes; completes assigned training as required.

• Assumes additional responsibilities as directed by CTSME Supervisor and/or other management.

• Identifies operational efficiencies and process improvements, contributing to an environment of continuous learning and improvement.

• Depending on level of experience, assists in training and mentoring of less experienced CT SMEs.

• Ensure the maintenance of a high personal level of knowledge concerning current regulation and changes within the clinical research industry by means of internal support and individual learning.

Your profile

• B.Sc. (Hons) in life science or equivalent.

• Minimum 2-3 years' experience as a CRA/site coordinator/study nurse within the clinical research industry

• Experience across different trial phases and therapeutic areas

• Excellent practical knowledge and understanding of the complexity of clinical trials and experience with different clinical trial systems/vendors

• Excellent analytical skills and attention to detail

• Ability to work independently as well as part of the project team, depending on the solution requirements

• Ability to produce accurate work within tight deadlines

• Knowledge of ICH GCP guidelines and experience in reviewing study-related documentation

• Excellent written and verbal communication in English

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