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Site Engagement Lead
On-site in Reading·Added 1 month ago (last checked 30 Oct)
Our summary
- Work mode
- On-site, Reading
- Contract
- Permanent
- Commute
- Cycle to work scheme
Skills
Nice to have
Requirements
What we're looking for
Please note, we require candidates that have at least 1 year of Site Engagement Lead (Site Care Partner, Clinical Research Lead, Clinical Trial Liaison type) experience.
Required qualifications and experience
- Bachelor's degree in life sciences or a related field.
- Extensive experience in clinical research, site management, or a related field required
- 1 year of experience as a Clinical Trial Educator/Site Engagement Lead/Clinical Trial Liaison type role
- 1 year of immunology experience; preferred dermatology
- Strong interpersonal and communication skills, with the ability to build rapport and establish effective working relationships with diverse stakeholders.
- Excellent organizational and problem-solving skills, with the ability to prioritize and manage multiple tasks simultaneously.
- Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Willingness to travel as required (approximately 6%)
Pay & benefits
What you'll get
- 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.
The role
What you'll 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.
SEL
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.
Fully sponsor dedicated
Working fully embedded within a pioneering, clinical-stage biotechnology organisation at the forefront of next-generation drug discovery, you will foster relationships with clinical trial sites, enhancing site engagement, and contribute to the advancement of innovative treatments and therapies.
Your Profile
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.
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
About ICON plc
ICON is a clinical research organisation (CRO) providing outsourced clinical development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company describes itself as the world's leading clinical research organisation and operates at global scale, with employees in 119 locations across 53 countries.
Its services span clinical and scientific operations, decentralised clinical trials, early clinical and laboratory services, medical imaging, regulatory affairs, consulting, commercialisation, medical writing, biometrics and outcome measures. ICON works across sectors including pharmaceuticals, biotech, medical devices and government and public health, and across therapeutic areas such as oncology, cardiovascular, central nervous system, vaccines and rare and orphan diseases.
- Industry
- Clinical research
- Headquarters
- Dublin, Ireland
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