ICON hiring Freshers as Clinical Research Associate I – Medical Affairs at BRAZIL

Clinical Research Associate I – Medical Affairs

About the role

A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity.

You will be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on our shared goals.

What you will be doing:

• Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs and study processes.

• Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations.

• Ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations and SOPs.

• Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate.

• Participates in audit preparation and follow-up activities as needed.

• May serve as preceptor, providing training to less experienced clinical team members.

You are:

• Bachelor’s degree in a health, life sciences or other relevant field of study.

• Previous experience supporting clinical trials including solid on-site monitoring experience.

• Travel is required.

• All employees must read, write and speak fluent English and host country language.

* Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above.

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