Cybersecurity Knowledge Associate: Regulatory Research

A global leader in applied safety science is seeking a UL GMA Knowledge Associate in Italy. The role involves completing comprehensive research reports, providing regulatory updates, and supporting business development by interpreting requirements and identifying new opportunities. Candidates should have at least two years of relevant experience and a high...

Role Overview As a UL GMA Knowledge Associate, you will: Complete comprehensive research reports of global requirements for any products under general supervision and mentorship. Provide global regulatory updates, research monitoring and document management of regulatory database. Support to interpret requirements to write executive summary reporting of...

Role OverviewAs a UL GMA Knowledge Associate, you will:Complete comprehensive research reports of global requirements for any products under general supervision and mentorship.Provide global regulatory updates, research monitoring and document management of regulatory database.Support to interpret requirements to write executive summary reporting of changes...

If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team...

The role of **Clinical Research Associate** is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the **CRA manager** the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting...

The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the monitoring plan,...

The role of Clinical Research Associate is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements...

**Job Description**: The role of **Clinical Research Associate** is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event...

The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and conducting on-site and remote monitoring visits in compliance with applicable regulatory standards (MDR, ISO 14155, ICH/GCP guidelines, Teleflex procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the monitoring plan,...

The Clinical Research Associate is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and...