Senior CRA (Unblinded)
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s integral expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Clinical Research Associate (CRA) at ICON Plc , you will support and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards, with a focus on Unblinded studies .
What You Will Do:
You will perform clinical trial monitoring activities requiring technical expertise, with a focus on quality, compliance, and continuous improvement.
Key responsibilities include:
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.




- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
- Providing support and guidance to site staff to maintain high standards of clinical trial conduct.
- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:
You will have a solid foundation in clinical trial monitoring, with specific experience working on Unblinded studies .
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field.
- At least 1 year of experience as a Clinical Research Associate working on Unblinded studies .
- Strong understanding of clinical trial processes, monitoring practices, and regulatory requirements.
- Proven ability to manage multiple sites and activities simultaneously, with strong organizational and problem-solving s

📌 Sr. CRA (Argentina)
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📍 Argentina