Job Description
Job Summary
We are seeking an experienced Project Manager in the Life Sciences domain to lead initiatives involving Veeva Vault platforms. The role requires close collaboration with cross-functional teams across the globe, ensuring successful delivery of regulatory, quality, and medical affairs programs.
Key Responsibilities
- Manage end-to-end delivery of Veeva Vault implementations and enhancements (RIM, QMS, Medical Affairs, etc.).
- Work closely with cross-functional global teams, including business, IT, vendors, and offshore partners.
- Develop and manage project plans, timelines, risks, issues, and dependencies.
- Facilitate project meetings, workshops, and status reporting in Japanese and English.
- Ensure compliance with Life Sciences and GxP regulations.
- Oversee change management, validation, and compliance documentation.
- Drive adherence to project governance, quality standards, and best practices.
Required Qualifications
- Minimum 5 years of Project Management experience in Life Sciences / Pharmaceutical environments.
- Proven experience with Veeva Vault modules such as RIM, QMS, and Medical Affairs.
- Strong understanding of regulatory, quality, and medical affairs processes.
- Business-level proficiency in Japanese and English (written and verbal).
- Demonstrated ability to manage global, cross-functional, and multicultural teams.
Preferred Qualifications
- PMP, PRINCE2, or equivalent certification.
- Experience working with Japanese pharma companies or global life sciences organizations.
- Knowledge of CSV, validation, and compliance standards
Are you interested in this position?
Apply by clicking on the “Apply Now” button below!
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