Safety Database Specialist / Clinical Trial Drug Safety Associate I

About the role

Everest is seeking a Safety Database Specialist / Clinical Trial Drug Safety Associate I to support Argus Safety database operations for clinical trials. The role is based in Sofia, Bulgaria and involves both database development and administration to meet drug safety objectives.

Key responsibilities

• Support day‑to‑day operation of Argus Safety, focusing on database development and administration.
• Configure Argus Safety for new clients, products, and studies across development, validation, and production environments.
• Manage user privileges and workflow settings, and perform post‑go‑live database modifications.
• Maintain and update technical specifications documentation (Configuration Specifications Document) for each change control.
• Develop UAT scripts for new builds or modifications and lead UAT validation activities.
• Review protocols and reference materials to contribute to project timelines and ensure good project management practices.
• Assist Pharmacovigilance and Drug Safety teams in planning, directing, and managing safety database development and maintenance.

Required profile

• Committed, skilled, and customer‑focused individual.
• Ability to work collaboratively with safety and pharmacovigilance teams.
• Strong attention to detail and documentation accuracy.

Required skills

• Argus Safety
• Database configuration and administration
• UAT script development
• Technical specifications documentation