- Develop an innovative strategy for the regulatory solution (product and services) in both document management of publishing
- Define the requirements for the solution and work with different teams to execute on the strategy
- Develop marketing materials to promote the extended regulatory offering
- Work with sales to find early adopters for the solution and future prospects
- Interact with customers and prospects in both sales and implementation phase of the project
- Keep up to date on regulations related to eCTD, NeeS and other standards on a global basis and identify required changes in the solution over time
Experience
- Detailed knowledge of requirements related to publishing, eCTD, NeeS and other standards
- Have a detailed understanding of the overall requirements in regulatory publishing and document management
- Preferably worked on or with applications in these areas
- Familiar with the Pharmaceutical Industry in general
- Able to work independently
- Able to travel up to 50% of time including to Europe and US
- Fluent in English
Competencies : (Competencies requirement for the candidate to perform the task)
- Excellent Communication (Writing and Verbal)
- Customer Focused
- Organization Skills
- Drive to deliver superior quality proposals
- Strong Time management
- Good Stakeholder management
- Strong Project management and tracking
- Excellent MS-Office skills
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