Site Engagement Liaison
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Site Engagement Liaison at ICON, you will foster relationships with clinical trial sites, enhancing site engagement, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- Building and maintaining strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff.
- Providing support and guidance to site staff on study protocols, procedures, and regulatory requirements, ensuring compliance and successful study conduct.
- Identifying opportunities to improve site engagement and optimize site performance through regular communication and feedback mechanisms.
- Collaborating with internal teams to develop and implement site engagement strategies tailored to the specific needs of each study and site.
- Monitoring site performance metrics and providing regular updates to study teams on site engagement activities and outcomes.
Your Profile:
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
- Bachelor's degree in Life Sciences or a related field.
- At least 5 years of experience as a CRA/Senior CRA; CTM experience preferred.
- Solid experience managing complex clinical trials across Oncology and non-Oncology therapeutic areas.
- Demonstrated experience in study start-up, site activation, study conduct, and close-out activities.
- Strong study oversight and site management experience, including prior experience as a site monitor/CRA.
- Experience reviewing Monitoring Visit Reports (MVRs) and driving appropriate follow-up actions.
- Strong knowledge of ICH-GCP, quality standards, and applicable regulatory requirements.
- Strong quality mindset, with a commitment to compliance and inspection readiness.
- Excellent communication, stakeholder management, teamwork, organizational, and problem-solving skills.
- Fluent in English and Hebrew, with willingness to travel as required (approximately 60%).
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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