Site Engagement Liaison

ICON; Argentina; Presencial; ARS 78.500.000 - 104.667.000; Jornada completa

Descripción de la vacante

A leading global clinical research organization is seeking a Site Engagement Liaison to enhance relationships with clinical trial sites. Responsibilities include providing support on study protocols, optimizing site performance, and collaborating with internal teams on engagement strategies. The ideal candidate has a background in life sciences and strong interpersonal skills. This role offers a competitive salary and comprehensive benefits, including health insurance and retirement planning.

Servicios

Various annual leave entitlements

Health insurance options

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Formación

• Prior experience as a site monitor, in start-up activities, and close-out activities.
• Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.

Responsabilidades

• Build strong relationships with key stakeholders at clinical trial sites.
• Support site staff on study protocols and regulatory requirements.
• Identify opportunities to improve site engagement.

Conocimientos

Interpersonal skills

Communication skills

Organizational skills

Problem-solving skills

Educación

Bachelor's degree in life sciences or a related field

Descripción del empleo

We are currently seeking a Site Engagement Liaison to join our diverse and dynamic team. As a Site Engagement Liaison at ICON, you will play a pivotal role in fostering relationships with clinical trial sites, enhancing site engagement, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

1. Building and maintaining strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff.
2. Providing support and guidance to site staff on study protocols, procedures, and regulatory requirements, ensuring compliance and successful study conduct.
3. Identifying opportunities to improve site engagement and optimize site performance through regular communication and feedback mechanisms.
4. Collaborating with internal teams to develop and implement site engagement strategies tailored to the specific needs of each study and site.
5. Monitoring site performance metrics and providing regular updates to study teams on site engagement activities and outcomes.

Your profile

• Bachelor's degree in life sciences or a related field.
• Demonstrated prior experience as a site monitor, in start-up activities, and close-out activities. Knowledge of quality and regulatory requirements.
• 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.

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 include:

• Various annual leave entitlements
• A range of health insurance options 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, TELUS Health, offering 24-hour access to a network of over 80,000 professionals for support
• 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 website to learn more about working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion and belonging are fundamental to our culture. We are committed to providing an inclusive, accessible environment for all candidates. ICON ensures a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If you need a reasonable accommodation during the application process or to perform the essential functions of a position, please let us know through this form.

Interested in the role but unsure if you meet all requirements? We encourage you to apply — you might be exactly what we’re looking for at ICON, whether for this or other roles.