Senior Consultant - Regulatory Operations Software Implementation Remote
Senior Consultant - Regulatory Operations Software Implementation Remote
Posted on :
07-04-2025
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1 Vacancy
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Monthly Salary
$ 80000 - 200000
Vacancy
1 Vacancy
Posted on :
07-04-2025
Job Description
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.
At the heart of Veeva are our values: Do the Right Thing Customer Success Employee Success and Speed. Were not just any public company we made history in 2021 by becoming apublic benefit corporation(PBC) legally bound to balancing the interests of customers employees society and investors.
The Role
We are looking for an experienced consultant with deep expertise in navigating customers through complex software implementation. 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.
Veeva Systems is looking for consulting leaders with system implementation experience and a passion for helping customers optimize their regulatory data and document management processes.
As a key member of our Professional Services team the Senior Consultant will be responsible for understanding our customers global regulatory needs translating requirements into solution design and defining global strategies for deploying 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
- Lead 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
- Manage software implementation projects and customers through the full implementation lifecycle including project planning requirements gathering migration configuration validation and golive activities
- Conduct configuration requirements workshops then design prototype configure and thoroughly document content solutions. Think critically about business requirements to ensure the solution reflects business requirements and focuses on Veeva best practices customer success and longterm adoption
- Guide our customers and internal team with program and project management including resource planning leading and motivating the crossfunctional team
- Serve as the primary customer liaison managing communication risks and project reporting between the project team customer and internal stakeholders
- Mentor project team and consultants with a focus on continuous growth
- Collaborate crossfunctionally with Product Strategy Sales and other teams across Veeva
Requirements
- 8 years experience working with or for organizations in life sciences or healthcare
- Direct technology system implementation maintenance or continuous improvement experience either as a consultant business or IT representative
- Proven track record leading highimpact system implementations and the ability to collaborate and manage diverse stakeholders and ensure delivery to a high degree of satisfaction
- Ability to act with speed to understand requirements technical abilities to create corresponding technical solutions and willingness to roll up your sleeves to design and implement a RIM solution
- Knowledgeable in life sciences compliance and computer systems validation requirements
- Typical travel is 25 but may be up to 50 based on customer requirements
Nice to Have
- Direct experience with systems such as Veeva Vault PAREXEL/LIQUENT InSight CSC Regulatory Tracker ArisGlobal Register OpenText SharePoint Documentum FirstDoc/FirstPoint NextDocs CARA Salesforce Workday Oracle SAP Lorenz Docubridge Extedo eCTD Manager Master Control Trackwise other regulatory information management or submission publishing systems etc.
- Consulting experience working with a major system integrator or software vendor in services delivery management and/or systems implementation
- Regulatory Affairs Regulatory Operations or Pharmacovigilance background including indepth knowledge of drug development processes and regulatory submissions; including Labeling Submission Publishing and/or Viewing systems
- experience with Agile methodology and/or ACP Certification
- SaaS/Cloud experience
Perks & Benefits
- Medical dental vision and basic life insurance
- Flexible PTO and company paid holidays
- Retirement programs
- 1 charitable giving program
Compensation
- Base pay: $80000 $200000
- 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.
#LIRemote
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.
Required Experience:
Senior IC
Employment Type
Full-Time
Key Skills
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