Sr. Manager, Veeva Vault Systems Administration
Remote (United States)
Job Description Summary:
The Senior Manager, Veeva Vault System Administrator primary duty is to improve business processes with technology and provide local functional and process support. The candidate will provide functional and technical support, incident management, instance administration, release management, upgrade support, testing, as well as end user training to the business. Candidates must have a solid understanding of Veeva Vault, especially eTMF, Regulator, Quality, PromoMats and MedComms. These are power user types of roles, with some level of functional understanding of the implemented design, leveraging project and process support documentation and resources. Candidate must be self-directed, be a great team player, and have excellent communication skills to be considered for this role. This person works cross-functionally with internal departments and external resources on system and business process related issues. Preference given to those candidates who have experience in life sciences or FDA regulated industries.The Senior Manager, Veeva Vault System Administrator ensures adherence to relevant regulatory requirements (e.g. 21 CFR Part 11 / EU Annex 11) and company Standard Operating Procedures (SOPs) as appropriate.
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Job Description:
ESSENTIAL FUNCTIONS
Primary duties/responsibilities:
Act as a Business Analyst, working with the business to understand business processes (clinical, regulatory, quality, medical and marketing) and requests for enabling appropriate solutions.
Extensive knowledge of document management systems
Extensive experience gathering & documenting business requirements
Solid understanding of Business Process Mapping, Business Requirements, Functional Requirements, Test Cases, User Guides and Admin Guides
Knowledge of Veeva Vault Platform
Familiarity with any of the following:
Quality business processes, such as electronic document management systems, document lifecycles, and / or change control, CAPA, Deviation, Audits/Inspections, Vendor Qualification business processes
Clinical business processes, such as electronic Trial Master File (eTMF) and / or clinical trial management systems (CTMS)
Regulatory business processes, such as regulatory document workflows, submissions, applications and / or registrations
Promotional and Medical materials
Support of end user Incidents
Configure enhancement requests in DEV, TEST and PRD environments and assist business users with troubleshooting and testing reported issues.
Liaise with Managed Service Provider or software vendor, as applicable
Provide relevant support for audit/inspection requests related to Veeva Vault systems.
Ad hoc data and document loads using Vault Loader and Vault File Manager as per business needs
Change Management processes; validation and Good Documentation Practices
Vault Reporting capabilities
Solid understanding of Vault security profiles and permission sets
Working knowledge of Vault Connectors and understanding of Vault-to-Vault transfers.
Veeva certifications desired
Understand and support master data governance for business processes.
Respond to requests for power user support and be available to address Tier 1 support (process support, master data, user access, user support and other non-technical issues)
Maintain current knowledge base of solutions and work with Tier 2 and 3 support sustainment teams to facilitate technical break / fixes.
Ability to prioritize and juggle multiple concurrent projects and day-to-day requests.
KNOWLEDGE/SKILLS/ABILITIES REQUIRED
* Minimum level of education and years of relevant work experience.
A Bachelor's degree in Computer Science, Information Systems or other related field and a minimum of 5 years in a pharmaceutical, biotechnology or other regulated environment OR equivalent experience and/or education.
* Special knowledge or skills needed and/or licenses or certificates required.
5+ years of relevant Veeva Vault System Administrator experience, specifically with Clinical, Regulatory and / or Quality Vaults
Advanced skill level with Microsoft Office, especially Excel, Word, PowerPoint, and Outlook
Excellent verbal and written communication and training skills, and patience
Ability to read, understand, and follow complex instructions
People-oriented -- enjoys interacting with people and working on group projects
Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.
Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.
* Travel requirements
Up to 10% travel
Expected Base Salary Range:
$131,800 - $155,000. The base salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity.
In addition to base salary, PTC employees are also eligible for short- and long-term incentives. All eligible employees may also enroll in PTC’s medical, dental, vision, and retirement savings plans.
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EEO Statement:
PTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.
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- End user training
- Gather and document business requirements
- Improve business processes
- Incident management
- Instance administration
- Provide functional and technical support
- Release Management
- Support audit/inspection requests
Admin Guides Audits Biotechnology Business process mapping Business Requirements CAPA Change Control Clinical Trial Management Clinical trial management systems Communication Data Governance Document management Document management systems ETMF Functional Requirements Master data governance Medcomms Microsoft Office Pharmaceutical Problem-solving Promomats Quality Regulatory Regulatory Document Workflows Regulatory requirements Technical Support Test Cases Troubleshooting User Guides Vault Connectors Vault File Manager Vault Loader Vault Security Profiles Veeva Veeva Vault
Experience5 years
Education Certifications TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9