Veeva Systems is a missiondriven organization and pioneer in industry cloud helping life sciences companies bring therapies to patients faster. As one of the fastestgrowing SaaS companies in history we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.
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.
Veevas RIM suite is the industrys 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 cloudbased 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 cloudbased 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.
What Youll Do
Guide life science customers in the configuration and implementation of Veevas 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 crossfunctional 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 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
Medical dental vision and basic life insurance
Flexible PTO and company paid holidays
Retirement programs
1 charitable giving program
Compensation
Base pay: $65000 $145000
The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications experience and expected contributions. This position may also be eligible for other types of compensation in addition to base salary such as variable bonus and/or stock bonus.
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Veevas headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.
Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color sex sexual orientation gender identity or expression religion national origin or ancestry age disability marital status pregnancy protected veteran status protected genetic information political affiliation or any other characteristics protected by local laws regulations or ordinances. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process please contact us at.
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