Senior Consultant, MedTech RIM

September 29

🔔 Pennsylvania – Remote

Although this job is listed in Pennsylvania, this company may be open to hiring remote in other states.

💵 $80k - $200k / year

⏰ Full Time

🟠 Senior

💼 Consultant

🦅 H1B Visa Sponsor

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Veeva Systems

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SaaS • Healthcare Insurance • Pharmaceuticals

Veeva Systems is a cloud-computing company focused on the global life sciences industry. It provides software, data, and consulting services to streamline research and development, quality management, regulatory operations, and commercial processes. Veeva's solutions encompass clinical trials, regulatory submissions, drug safety management, and commercial execution to support life sciences enterprises in their mission to improve and extend life.

1001 - 5000 employees

☁️ SaaS

⚕️ Healthcare Insurance

💊 Pharmaceuticals

📋 Description

• Lead MedTech customers through their regulatory transformation via the implementation of Veeva RIM applications • Partner with customer SMEs and business leaders to analyze, develop, and implement Regulatory processes that solve business problems and support business needs with the Veeva RIM (Submissions, Submissions Archive, Registrations, and Publishing) • Analyze and document current state business processes, identifying pain points and gaps in process or system functionality as areas of opportunity. • Define roll-out strategies for deployment of Veeva RIM across global Regulatory teams • Serve as the primary customer liaison managing communication between project team, customer, and other internal stakeholders • Represent Professional Services across multiple engagements and workstreams (e.g., solution design and configuration, data migration, systems integration, etc.) • Mentor project team and junior consultants in the Professional Services organization

🎯 Requirements

• 8+ years of experience implementing regulatory information management systems and processes e.g. Registration Data Tracking Systems, Submission systems, creating business processes to address global regulatory requirements • Working knowledge of life sciences compliance, regulatory guidance, day in the life business processes • Ability to quickly understand business use cases and opportunities for change, to create corresponding process and business improvements ensuring that they align with Preferred Vault Practices • Experience implementing software systems with the ability to comprehend and translate business requirements and create corresponding solutions designs • Proven expertise in customer leadership and mentoring of team member • Demonstrated work history in stakeholder management, critical thinking skills, ability to conduct complex and technical communications in a wide variety of settings and audiences, and the determination to see client success with solution implementation • Ability to travel up to 50% • Nice to Have: Direct experience with systems such as Veeva Vault, PARAXEL/LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, IQVIA, Trackwise, or other regulatory information management systems • Nice to Have: Consulting experience, working with a major software vendor or process management consulting group • Nice to Have: Regulatory Affairs, Regulatory Operations, or Submissions Management background • Nice to Have: Consulting experience • Nice to Have: Life Science, computer science, biochemical and mechanical engineers or related degree • Nice to Have: SaaS/Cloud experience

🏖️ Benefits

• Medical, dental, vision, and basic life insurance • Flexible PTO and company paid holidays • Retirement programs • 1% charitable giving program • Work Anywhere: flexibility to work from home or in the office • May be eligible for variable bonus and/or stock bonus