Medical Research Professional

hace 3 días


Santiago, Metropolitana, Chile ICON A tiempo completo
Senior Clinical Research Associate Role at ICON

About the Opportunity:

We are seeking a highly skilled and experienced Senior Clinical Research Associate to join our team at ICON. As a key member of our clinical research organization, you will be responsible for monitoring and managing clinical trials to ensure data integrity and patient safety.

About You:

To be successful in this role, you will require a Bachelor's degree in a health-related field and a minimum of 2 years of experience in on-site monitoring, preferably in oncology. You must also have excellent communication and interpersonal skills, as well as the ability to work independently and as part of a team.

The Role:

Your primary responsibilities will include completing onsite and remote monitoring activities in accordance with ICH-GCP guidelines and applicable regulations. You will also verify the protection of study participants by confirming informed consent procedures and protocol adherence. Additionally, you will ensure the integrity of clinical data and write and submit reports of investigational site findings.

Salary and Benefits:

We offer a competitive salary of $85,000 per annum, commensurate with experience, plus a range of benefits including comprehensive health insurance, retirement savings plan, and opportunities for professional development. Our diverse and inclusive workplace culture values innovation, collaboration, and employee well-being.

Why Join Us?

At ICON, we prioritize diversity, equity, and inclusion, recognizing that a rich and diverse workforce drives innovation and improves patient outcomes. We strive to create an environment where everyone feels valued, empowered, and supported to reach their full potential. If you're passionate about delivering high-quality clinical research services and contributing to a dynamic team, we encourage you to apply for this exciting opportunity.



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