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consulting project management life sciences veeva regulatory information management📋 Description
- Guide life sciences customers in configuring and implementing Veeva Regulatory Suite
- Lead configuration workshops, design, document, prototype, and deploy solutions
- Program and project management, including resource planning and cross-functional leadership
- Communicate between the project team, customer, and internal stakeholders
🎯 Requirements
- 3+ years in life sciences or healthcare as consultant, business, or IT
- Technical ability to design, configure, and implement a RIM solution
- Excellent collaboration and communication with diverse stakeholders
- Team player with strong organization skills and speed in complex environments
- Ability to travel 25-50% as required
- Consulting experience with a major system integrator or software vendor
- Knowledge of drug development, Regulatory Affairs, or Regulatory Operations
- Experience in life sciences compliance and computer systems validation
🎁 Benefits
- Health and wellness programs
- Life Assurance
- Veeva charitable giving program
- Additional annual leave over Christmas break
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