Open role
[Remote] Veeva Administrator
Note: The job is a remote job and is open to candidates in USA. RxCloud is hiring a Veeva Administrator to maintain its Veeva Vault applications in a compliant manner. The role administers Regulatory Information Management, document, training, Quality Management, and Laboratory Information Management systems, and supports their ongoing maintenance and improvement.
Responsibilities
- Serves as the Veeva Business Administrator responsible for the implementation, management, and ongoing maintenance of the Veeva Vault, including documents, training, QMS, LIMS, and RIMs
- Coordinates with business process owners for change control, quality assessment, and approval, testing, and deployment
- Develops and implements ongoing training
- Creates and maintains user accounts
- Ensures controls related to approval levels and user access are established and maintained
- Manages changed static data
- Proactively identifies and works to resolve project and system issues
- Ensures Veeva Vault conforms to regulatory requirements
- Oversees and participates in the development of application documentation
- Ensures system workflows and triggers are developed and maintained as established by business process owners
- Works with business stakeholders to develop and prepare reports, metrics, and dashboards
- Works closely with various business stakeholders to lead and manage business requirements and system solution delivery
- Supports ongoing maintenance and enhancements as required
- Assesses changes to the system (e.g. new releases) for business and training impact
- Drive improvements and efficiencies
Skills
- A Bachelor's Degree in a related field plus 6 years of Quality, Regulatory, or System Administrator experience, or equivalent work experience is required
- Proven experience in leading and deploying a combination of the following: QMS, document management, Electronic Learning Management System, or Regulatory Information Management System
- Knowledge of Quality Assurance/Quality Control Operations and Regulatory
- Experience with system design and development from business requirements analysis to implementation and support
- Possess and demonstrate excellent oral and written communication skills and proactive problem-solving, analytical, and multi-tasking skills
- Possess the ability to work within a team-based environment while proactively forging positive relationships across all levels of management, departments, and suppliers
- Quality Systems Experience in a CGMP environment
- Excellent written/oral communication skills
- Self-motivated, flexible, and able to work in a small, fast-paced, dynamic, environment
- Experience in a pharmaceutical or any highly regulated environment is preferred
Benefits
- Remote work
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