Senior Clinical Research Professional

Há 3 dias

São Paulo, São Paulo, Brasil beBeeClinicalResearchAssociate Tempo inteiro

At ICON, we're seeking a talented Clinical Research Associate to join our diverse and dynamic team. As a key member of our team, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

The successful candidate will be responsible for monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. This will involve conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

You will also collaborate with cross-functional teams to ensure timely and accurate data collection and reporting. Additionally, you will provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.

The ideal candidate will have previous experience as a Clinical Research Associate I, with a strong understanding of clinical trial processes and regulatory requirements. They will also possess proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.

In return, we offer a competitive salary, along with a range of additional benefits designed to promote work-life balance and well-being. Our benefits include various annual leave entitlements, health insurance offerings, retirement planning opportunities, and more.

At ICON, inclusion and belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. If you need a reasonable accommodation for any part of the application process, please let us know.

So, if you're passionate about clinical research and looking for a new challenge, apply now to become a part of our dynamic team

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