Why this grade This listing scored 66/100, which is a C. It lost the most ground on pay transparency. See the breakdown
- Description depth 20 / 20 How much the posting actually says about the work, measured in characters of real text.
- Freshness 15 / 15 How recently it was posted. Older postings are likelier to be filled or abandoned.
- Pay transparency 12 / 25 A published salary range, worth more than any other single factor because it is what a candidate cannot find out without applying.
- Remote clarity 8 / 15 Whether "remote" means anywhere, or is quietly restricted to one country.
- Role specificity 6 / 10 Whether the listing is tagged well enough to tell what the role actually is.
- Corroboration 5 / 10 Whether more than one source carries this listing.
Every figure above is arithmetic over the posting itself — its salary field, its text, its age, its tags and how many sources carry it. How the grades work →
Mid level Full Time
The Role
Veeva is looking for Consultants with deep regulatory expertise and a passion for helping customers improve their process for Regulatory Information Management (RIM), submission management, publishing, and submission archiving. We want team members ready to challenge the status quo; you’re ready to transform businesses. 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. This is a remote, full-time permanent role with Veeva with a location preference in Hyderabad, Mumbai, Bengaluru, or Pune.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
Originally posted on Himalayas
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Where this listing came from
- 09 Oct 2026 Himalayas first sighting
Seen on 1 board over 0 days.