What You'll DoGuide life science customers in the configuration and implementation of Veeva's Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing) to streamline global regulatory processesLead configuration requirements workshops, design, and document, as well as prototype and deploy solutionsProgram and project management, including resource planning, leading and motivating a cross-functional teamCommunicate between the project team, customer, and internal stakeholdersRequirements3+ years experience working with or for organizations in life sciences or healthcare either as a consultant, business, or IT representativeTechnical abilities and willingness to "roll up your sleeves" to design, configure, and implement a RIM solutionAbility to collaborate and communicate excellently with diverse stakeholdersTeam player with strong organization skills and an ability to act with speed in a complex environmentAbility to travel as required by the businessNice to HaveConsulting experience, working with a major system integrator or software vendorKnowledge of drug development, Regulatory Affairs, or Regulatory OperationsExperience in life sciences compliance and computer systems validation requirementsPerks & BenefitsMedical, dental, vision, and basic life insuranceFlexible PTO and company paid holidaysRetirement programs1% charitable giving programCompensationBase pay: $65,000 - $145,000The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. RIM Implementation Consultant (Remote)Massachusetts - BostonProfessional Services - Services : R&D Svcs /Full-Time /RemoteApply for this jobVeeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.