Quality Systems (Veeva) Senior Consultant

This job is posted in multiple locations. When not at a client site, consultants work from their home office. Relocation is not required. 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. What You'll Do 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 How You'll Grow Receive the support and mentorship of your Clarkston colleagues and leaders Expand your existing skillset with internal and external professional development opportunities Travel is an integral part of this role and is estimated to average 30‑50%. This may vary based on client and project needs. When not traveling, consultants work from their home office. Relocation is not required. 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 Experience with regulatory information management systems, including registrations and submissions, preferred 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 Benefits Comprehensive Health and Wellness Benefits (Medical, Dental, Vision, and more) 401(k) 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 Clarkston Consulting is an equal opportunity employer. We are committed to ensuring our firm is rich in diverse skills, competencies, strengths, personalities, and culture. We foster an inclusive environment that embraces the unique contributions of our people to further our purpose. Please visit Diversity @ Clarkston to learn more about our diversity initiatives. #J-18808-Ljbffr Clarkston Consulting