
This 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 reviews 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. The role offers the appeal of contributing to meaningful patient health improvements while working within a collaborative global team. It is a remote position based in the US, providing flexibility for professionals seeking to develop their careers in pharmacovigilance.













