Volver

Sr Clinical Research Associate (Portugal)

CompraTica Empleos

EMP:Health
Portugal
Tiempo Completo
Remoto
0 vistas

Descripción

Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases.

GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development.

We operate as a private, profit-with-purpose company, channeling our commercial success back into scientific research, technology, and our people.

With approximately 700 people across multiple countries and three service lines, we are growing deliberately, and the capability of our leaders and our organization is central to how we get there.

If you want to do meaningful work, build something real, and invest back in research that changes lives — we want to meet you! Job Overview As a Senior Clinical Research Associate, you will play a key role in the successful delivery of clinical trials by independently managing clinical site monitoring and site management activities across Portugal and Spain, from study start-up through close-out.

You will act as a primary point of contact for investigative sites in these countries, ensuring compliance with protocols, ICH-GCP, applicable regulations and study.

Requisitos

while supporting high-quality patient data and study delivery

This is a senior individual contributor role with responsibility for supporting site performance, resolving issues, maintaining study documentation and providing guidance and mentorship to junior CRAs.

You will work closely with Clinical Operations, Project Management, sponsors and other cross-functional teams in a dynamic clinical research environment.

Responsabilidades

: Independently conduct and document onsite and remote monitoring activities, including site qualification, initiation, monitoring and close-out visits across Portugal and Spain
  • Ensure investigative sites comply with study protocols, ICH-GCP, applicable regulations, SOPs and project-specific requirements.

¿Te interesa? Aplicá ahora