Site Engagement Liaison

Pharmaceutical Research Associates, Inc; Argentina; Híbrido; ARS 80.620.000 - 107.494.000; Jornada completa

Descripción de la vacante

A leading research organization in Argentina is seeking a Site Engagement Liaison to drive project management for clinical operations. The ideal candidate will have at least five years of related experience and a degree in health or life sciences. Responsibilities include managing clinical deliverables and training clinical teams. This position offers a competitive salary and diverse benefits focusing on well-being and work-life balance.

Servicios

Various annual leave entitlements

Health insurance options

Retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible benefits like childcare vouchers and gym discounts

Formación

• 5 years of relevant experience in Clinical Operations roles.
• Onsite primary Lead CRA experience highly valued.
• Willingness to travel occasionally and be in the office at least twice per week.
• Fluent in English and host country language.

Responsabilidades

• Manage and prioritize clinical deliverables for quality and compliance.
• Create and administer clinical training plans.
• Recognize risks and establish contingency plans.
• Communicate effectively with project teams.
• Provide training and guidance to study team members.

Conocimientos

Clinical Operations Management

Risk Assessment

Training Skills

Effective Communication

Project Management

Educación

Bachelor’s degree in health or life sciences

Descripción del empleo

Overview

As a Site Engagement Liaison, you will play a key role in improving the lives of patients by accelerating the development of our customers' drugs and devices through innovative solutions.

Responsibilities

What you will be doing:

A Site Engagement Liaison is a single service project manager for clinical operations.

• Manages and prioritizes clinical deliverables to ensure quality, regulatory compliance, project timelines, budget, and sponsor expectations are met.

• Creates and administers clinical and site training plans, ensuring the clinical team understands responsibilities and performance standards.

• Recognizes potential risks within the study protocol and operational aspects of the trial; proactively establishes contingency and mitigation plans.

• Ensures quality standards and applicable regulatory requirements are met, facilitates internal audits and local health authority inspections as needed.

• Communicates effectively with sponsors, project managers, functional team leads, and other project members. Leads clinical study team meetings.

• Provides training and guidance to clinical study team members.

Qualifications

You are:

• Bachelor’s degree in health, life sciences, or a relevant field.

• 5 years of relevant experience in Clinical Operations roles, with onsite primary Lead CRA experience highly valued.

• Willing to travel occasionally and be in the office at least twice per week.

• Fluent in English and host country language, with the ability to read and write effectively.

• Equivalent education, training, and relevant experience may be considered.

What ICON can offer you:

Our success depends on the quality of our people. ICON values diversity, high performance, and talent development. In addition to a competitive salary, we offer a range of benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements
• Health insurance options
• Retirement planning options
• Global Employee Assistance Programme via TELUS Health
• Life assurance
• Flexible country-specific benefits such as childcare vouchers, gym discounts, and more

Visit our careers website to learn more: https://careers.iconplc.com/benefits

ICON is committed to inclusion and diversity, providing an accessible environment for all candidates. We ensure equal employment opportunities regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If you need accommodations during the application process, please let us know.

Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly what we’re looking for!