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life sciences regulatory submissions publishing veeva regulatory information management📋 Description
- Guide 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 processes
- Lead configuration requirements workshops, design, and document, as well as prototype and deploy solutions
- Program and project management, including resource planning, leading and motivating a cross-functional team
- Communicate between the project team, customer, and internal stakeholders
🎯 Requirements
- 3+ years experience working with or for organizations in life sciences or healthcare either as a consultant, business, or IT representative
- Technical abilities and willingness to “roll up your sleeves” to design, configure, and implement a RIM solution
- Ability to collaborate and communicate excellently with diverse stakeholders
- Team player with strong organization skills and an ability to act with speed in a complex environment
- Ability to travel (25% -50%) as required by the business
🎁 Benefits
- Health and wellness programs
- Life Assurance
- Veeva charitable giving program
- Additional annual leave over Christmas break
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