Safety Systems Analyst

• Supporting the maintenance of current pharmacovigilance safety system (ARGUS). and other GPS systems
• Ability to work flexible hours supporting users in different time zones. May need to work in shifts as needed/assigned.
• Collaboration with IT teams, Vendor resources to plan and implement system related changes (Routine changes and Change Requests). 
• Initiation, review and notification of routine changes to pharmacovigilance safety system.
• Review and analysis of user requirements prior to submission and implementation, participate in validation activities as required.
• Perform periodic review of administrator data including but not limited to user access, company product dictionary and Safety Data Exchange agreements.
• Ensure that changes made to the databases are controlled through the change control process.
• Ensure proposed changes to the Pharmacovigilance Safety System are reviewed and validated with GPS functional area prior to processing for implementation
• Responsible for creating, verifying and tracking complex change requests, including updates to reporting rules, product lists and code lists.
• Drive consistent interpretation of system related conventions, specifications, and definitions when making any configuration changes
• Maintain and manage SharePoint sites used for tracking systems requests (Routine changes and Change Requests)
• Take initiative to recognize, prioritize & escalate potential safety/ compliance issues
• Serve as a backup for the equivalent Data Analyst role as needed to generate complete and accurate reports from the pharmacovigilance safety system

Qualifications:

• Excellent technical, analytical and problem solving skills as it pertains to Pharmacovigilance database systems
• Strong knowledge of Pharmacovigilance system (e.g. ARISg, ARGUS) with good understanding of the database structure and application architecture
• Strong technical system skills (e.g. Word processing, Excel spreadsheets, Powerpoint, Sharepoint, SQL and Databases)
• Strong knowledge of pharmacovigilance terminology and understanding of data entry conventions
• Excellent oral and written communication skills with attention to detail
• Excellent interpersonal skills that encourage teamwork
• Ability to work independently under strict deadlines and changing priorities
• Ability to multitask and prioritize changing workload for self
• Broad knowledge/understanding of relevant ICH guidelines, as well as FDA and EU Regulations
• Problem Solving- Identify priorities and key issues in complex situations, and formulate and execute issue resolution with minimal assistance