Empleos de Ctis

This role involves providing strategic regulatory expertise and leadership for clinical trial applications, with a focus on EU Clinical Trials Regulation (CTR) submissions and Clinical Trials…

PVpharm is seeking a Senior Pharmacovigilance Specialist to manage complex PV projects, handle adverse events, and support regulatory compliance.

This role involves advising project teams on regulatory requirements for clinical studies in Europe, preparing and submitting regulatory applications, and managing documentation and site interactions.

Rho Inc is hiring a Study Start Up Lead to manage the study start up process through site activation, coordinating with project managers and clinical trial leads.