Latam Clinical Research Specialist — Remote Impact

IQVIA Inc; Quilmes; Híbrido; ARS 1.000.000 - 1.500.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid work model

Competitive benefits

Descripción de la vacante

ICON is a global healthcare intelligence and clinical research organisation. This hybrid role in Argentina supports site management to ensure trials are conducted efficiently, compliantly, and to the highest quality standards, helping patients access new medicines faster.

You will activate sites, review essential documents, track approvals, coordinate visits, keep systems up to date, support payments, and drive improvements with internal teams, with travel around 10%.

Formación

• Bachelor's degree or equivalent experience in life sciences, healthcare, business, or related field.
• Initial experience in clinical research, administration, or a regulated environment is preferred.
• Strong organisational skills with ability to manage multiple tasks, priorities and deadlines.
• High attention to detail and accuracy in documentation and data entry.
• Effective written and verbal communication with a customer-focused approach to site support.
• Proficiency with MS Office and comfort with electronic systems and databases.

Responsabilidades

• Support site activation activities, including collection, review, and tracking of essential documents and approvals.
• Maintain up-to-date site information in clinical trial management systems and trackers.
• Assist CRAs and project teams with site communications, follow-up, and resolution of site-level queries.
• Coordinate logistics for site visits and meetings, including scheduling and documentation preparation.
• Ensure accurate filing and maintenance of essential documents to support inspections and audits.
• Collaborate to support timely site payment processing and issue resolution.
• Contribute to process improvements and share best practices to enhance site support efficiency.

Conocimientos

Organisational skills

Attention to detail

Communication skills

MS Office proficiency

Team collaboration

Travel availability

Educación

Bachelor's degree in life sciences, healthcare, business, or related field

Herramientas

MS Office

Electronic systems/databases

Descripción del empleo

Hybrid role / 3 Days at the office Bs As
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Clinical Site Associate at ICON, you will support site management activities and ensure that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.

What You Will Do

• Supporting site activation activities, including the collection, review, and tracking of essential documents and approvals.
• Maintaining up-to-date site information and status in clinical trial management systems and trackers.
• Assisting CRAs and project teams with site communications, follow-up, and resolution of site-level queries.
• Coordinating logistics for site visits and meetings, including scheduling, documentation preparation, and follow-up actions.
• Ensuring accurate filing and maintenance of essential documents to support inspection and audit readiness.
• Collaborating with internal stakeholders to support timely site payment processing and issue resolution.
• Contributing to process improvement initiatives and sharing best practices to enhance site support efficiency.

Your Profile

• Bachelor's degree in life sciences, healthcare, business, or a related field, or equivalent experience.
• Initial experience in clinical research, administration, or a similar regulated environment is preferred.
• Strong organisational skills with the ability to manage multiple tasks, priorities, and deadlines.
• High attention to detail and accuracy in documentation and data entry.
• Effective written and verbal communication skills, with a customer-focused approach to site support.
• Proficiency with MS Office and comfort working with electronic systems and databases.
• Ability to work collaboratively in a team environment and adapt to changing priorities.
• Willingness to travel as required (approximately 10%).

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.

• 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.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive ... 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.