As a Senior Clinical Research Associate, you will monitor clinical trial programs and manage regional clinical trial sites to support biological and pharmaceutical developmental programs in a manner consistent with relevant regulations including ICH/GCP and PhRMA guidelines along with Catalyst Clinical Research’s applicable SOPs and working practices. You will collaborate with an assigned clinical research team to provide input on site selection, study initiation procedures, conflict resolution, and audit responses. You will effectively communicate all relevant and important findings with appropriate in-house personnel.
