Vacancy expired!
- Direct administration of the Veeva Regulatory and Clinical SaaS platforms creating and managing object records, templates, content plans, and mastered data elements (e.g., List of Values) for TRI client research
- Access management through administration of users, groups, and security roles including external access
- System and client configuration through establishing document types, fields, lifecycles as well as supporting automation through workflows and notification management
- Solid understanding of clinical research relating to operations (especially site essential document collection and sponsor trial master file requirements) and regulatory services (especially IND study submissions planning for FDA, EMA, and other regulatory authorities).
- Knowledge of Veeva's system objects and architecture, including the Advanced Data Model describing metadata and relationships between objects (e.g., documents, studies, dossiers, etc.). Significant experience in other commercial leading eTMF and Regulatory Information Management platforms may be considered, but Veeva is strongly preferred
- Functional database query/SQL skills required for evaluating upstream or downstream document repositories
- Competitive pay based on years of experience: $70,000-$85,000
- Full benefits: Health, Medical, Vision, Dental (Cigna); 401K
- ID: #49971597
- State: Maryland Columbia 21044 Columbia USA
- City: Columbia
- Salary: USD TBD TBD
- Job type: Permanent
- Showed: 2023-05-20
- Deadline: 2023-07-18
- Category: Admin/office