Quality Systems (Veeva) Senior Consultant

Clarkston Consulting • Raleigh, NC

8d • Hybrid

About The Position

Clarkston Consulting is seeking motivated, self-driven leaders who are energized by team results and interested in joining a firm that values its culture and people as its biggest strengths. Come join us as a Quality Systems (Veeva) Senior Consultant, and in this role, you will deliver creative business solutions to our market-leading clients in the life sciences, consumer products, and retail industries. Together, we can find the answers to our clients' most challenging business problems through a combination of our industry expertise, business process knowledge, and consulting excellence.

Requirements

• 5+ years of experience working with or for life sciences companies
• Experience implementing Document or Quality Management systems for life sciences as a consultant, business, or IT representative
• Understanding of global quality requirements, compliance considerations, and processes
• Firsthand experience with systems such as Veeva Vault, EtQ, TrackWise, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, or other quality information or content management systems
• Team Lead experience
• Flexibility and adaptability - our consultants work on everything from design to hands-on configuration and can stretch into new roles
• Thorough client services orientation and accustomed to taking an active role in executing engagements and project plans/tasks
• Excellent analytical skills and the ability to present and write at publication quality level to communicate findings and recommendations
• 4-year degree from an accredited college or university

Nice To Haves

• Experience with regulatory information management systems, including registrations and submissions, preferred

Responsibilities

• Participate in projects at life sciences and consumer products companies designing and deploying Veeva
• Support the configuration and implementation of Veeva Quality suite and Veeva Vault RIM capabilities
• Lead requirements workshops, design, prototype, configure and document content management/QMS data solutions
• Earn trusted client status and develop relationships that extend beyond the project’s life cycle
• Create and oversee project or workstream plans and timelines, define deliverables, assign team roles and resources, identify and track issues and their resolution, and help manage project scope and requirements.
• Assist in validation of computer systems for use in a Good Manufacturing Practices (GMP) environment and creating and revising Standard Operating Procedures (SOPs)
• Conduct knowledge transfer and training of end-users, including sharing best practices
• Provide guidance to junior systems analysts and client personnel assigned to projects

Benefits

• Comprehensive Health and Wellness Benefits (Medical, Dental, Vision, and more)
• 401k with company contributions
• Paid vacation, personal days, holidays, and sick leave
• Paid Parental Leave and Family Building Benefits (Adoption, Surrogacy, and Infertility Support)
• Life and Disability Insurance
• Training and Professional Development investments, Tuition Assistance, and more

What This Job Offers

• Job Type: Full-time
• Career Level: Senior