
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, conducting literature reviews to identify safety signals, managing regulatory submissions, and maintaining compliance with international pharmacovigilance standards. This position appeals to professionals seeking to make a meaningful impact on patient health while developing their career in a collaborative, global environment. The role offers the flexibility to work remotely from the US, allowing for a balanced work arrangement while contributing to critical safety operations and regulatory intelligence.













