
The Patient Safety Associate I role at Parexel supports global drug safety and post-marketing surveillance activities within the Clinical Research Organization. Key responsibilities include processing Individual Case Safety Reports with high accuracy, conducting literature searches to identify safety signals, and assisting with regulatory submissions and aggregate report development. The position requires strong attention to detail and knowledge of pharmacovigilance principles to ensure compliance with international regulations. This opportunity appeals to professionals seeking to make a meaningful impact on patient health while working in a collaborative, global team environment. The role offers the flexibility to work remotely from the United States, providing a balanced work arrangement for those dedicated to advancing clinical research and safety standards.









