Site Management Associate I - Buenos Aires, Argentina - ICON plc

ICON plc

Empresa verificada

Buenos Aires, Argentina

hace 2 semanas

Publicado por:

Sofía Rodríguez

beBee Recruiter

Descripción

At ICON, our strength lies in our people. Our diverse teams make us a better partner to our customers and help us achieve our mission of advancing and enhancing patients' lives.

Embedded in our 'Own It' culture are four core values that unite us as individuals and distinguish us as an organization: Accountability & Delivery, Collaboration, Partnership, and Integrity.

Our aspiration is to stand out as the top Clinical Research Organization in providing exceptional service to our clients and patients at every interaction - striving to be the preferred partner in drug development.

This encompassing vision drives us forward, and we are searching for skilled individuals who align with this purpose.

If you possess the same determination, come join our team. You'll be immersed in a vibrant and supportive setting alongside some of the brightest and most amicable professionals in the industry, playing a pivotal role in shaping the field.

Overview

Role Overview: this position offers comprehensive support to study sites and clinical project teams involved in research studies, ensuring compliance with protocols, SOPs, and regulatory requirements.

Responsibilities:

Complete essential document collection and review across the study lifecycle, including site activation, maintaining the site's clinical trial master file.
Serve as the primary contact for study sites, handling inquiries, managing supplies, and conducting monitoring visits.
Ensure timely and accurate data entry, perform data reviews, and address follow-up tasks.
Conduct risk assessment and management activities throughout the project, complying with guidelines and SOPs.
Handle various essential document collection, review, negotiation, and submission tasks under supervision.
Submit notifications to regulatory authorities and oversee clinical data review and query resolution.
Maintain study documentation in relevant systems per project protocol and SOPs.

You will need:

Familiarity with TMF or clinical trial management systems.
Minimum of 2 years experience in similar roles.
Proficiency in English - reading, writing, and speaking.
Intermediate Excel skills.
Health Sciences degree.

Note:

This is a Hybrid Position.

Benefits of Working in ICON:

Our achievements hinge on the caliber of our workforce. We prioritize cultivating a culture that recognizes excellence and fosters talent.

We offer competitive salary packages and regularly compare them with industry standards. Our annual bonuses reflect performance achievements, rewarding both company and individual goals.

In addition to a variety of health benefits for employees and their families, we provide competitive retirement plans and life assurance for future security.

But beyond the financial rewards and perks, you'll experience an environment that empowers you to fulfill your purpose and inspire enduring change.

ICON advocates for equal opportunities and inclusivity and is dedicated to maintaining a workplace free from discrimination and bias, ensuring that all applicants are considered fairly for employment.