Consultant - Veeva RIM Professional Services
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Strong ghost-posting signals
- open for 128 days (90+ without a fill is a strong ghost signal)
- reposted 1× (reposts correlate with ghost postings)
- removed from the board and reposted at least once
- 783 open roles at this company in 30 days (mass-hiring blitz)
- no salary disclosed (correlates with ghost postings)
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About the role
What You'll Do
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
Nice to Have
Consulting experience, working 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 requirements
Perks & Benefits
Health and wellness programs
Life Assurance
Veeva charitable giving program
Additional annual leave over Christmas break
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