Think critically about business requirements to ensure the solution reflects business requirements and focuses on Veeva best practices, customer success, and long-term adoptionGuide our customers and internal team with program and project management including resource planning, leading, and motivating the cross-functional teamServe as the primary customer liaison managing communication, risks, and project reporting between the project team, customer, and internal stakeholdersMentor project team and consultants with a focus on continuous growthCollaborate cross-functionally with Product, Strategy, Sales, and other teams across VeevaRequirements8+ years experience working with or for organizations in life sciences or healthcareDirect technology system implementation, maintenance, or continuous improvement experience either as a consultant, business, or IT representativeProven track record leading high-impact system implementations and the ability to collaborate and manage diverse stakeholders and ensure delivery to a high degree of satisfactionAbility to act with speed to understand requirements, technical abilities to create corresponding technical solutions, and willingness to "roll up your sleeves" to design and implement a RIM solutionKnowledgeable in life sciences compliance and computer systems validation requirementsTypical travel is 25% but may be up to 50% based on customer requirementsNice to HaveDirect experience with systems such as Veeva Vault, PAREXEL/LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, Documentum, FirstDoc/FirstPoint, NextDocs, CARA, Salesforce, Workday, Oracle, SAP, Lorenz Docubridge, Extedo eCTD Manager, Master Control, Trackwise, other regulatory information management or submission publishing systems, etc. Consulting experience, working with a major system integrator or software vendor in services delivery management and/or systems implementationRegulatory Affairs, Regulatory Operations, or Pharmacovigilance background including in-depth knowledge of drug development processes and regulatory submissions; including, Labeling, Submission Publishing, and/or Viewing systemsExecution experience with Agile methodology and/or ACP CertificationSaaS/Cloud experiencePerks & BenefitsMedical, dental, vision, and basic life insuranceFlexible PTO and company paid holidaysRetirement programs1% charitable giving programCompensationBase pay: $80,000 - $200,000The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role.