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# RIM Implementation Consultant

- **Company:** Veeva's Headquarters
- **Location:** San Francisco, CA, United States (Remote available)
- **Experience:** Experienced
- **Salary:** $65,000.0 - $145,000.0
- **Contract:** Permanent contract
- **Skills:** Document Management Systems, Information Management, Information Technology, Veeva
- **Published:** September 4, 2026
- **Apply:** https://startup.jobs/rim-implementation-consultant-veevasystems-6391329

## About the Role

* 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 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
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## Description

Veeva Systems is looking for individual leaders with consulting and system implementation experience and a passion for helping customers optimize their regulatory data and document management processes.
Veeva's RIM suite is the industry's only unified software solution that provides fully integrated regulatory information management (RIM) capabilities, including data and document management, submission publishing, and archival on a single cloud-based platform.
As a member of our Professional Services team, you will be responsible for understanding our customers' global regulatory needs, translating requirements into solution design, and configuring our cloud-based solution for managing regulatory information across the enterprise.
Opportunities are available within the United States for this role, which is a remote position with a preference for Eastern or Central Time Zone. If a candidate is in close proximity to an airport and able to meet travel requirements, there is no work location requirement. Qualified U.S.-based candidates are encouraged to apply., * 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


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