Teams at Allen Spolden

The role involves ensuring quality in adverse event report processing, collaborating with teams, conducting training, and maintaining regulatory compliance in pharmacovigilance.

Support clinical research activities, design protocols, generate SOPs, monitor studies, and prepare reports under supervision. Requires attention to detail and communication skills.

Support planning and execution of clinical trials by coordinating site communication, maintaining TMF and regulatory documents, tracking milestones, assisting data management and study start-up, and ensuring ICH-GCP and SOP compliance.