FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Tech Stack
Tools & technologiesPMPVault
About the role
Key responsibilities & impact- Lead global regulatory strategy development, ensuring compliance with FDA, EMA, MHRA, PMDA, and other health authorities
- Provide expert guidance on regulatory submissions, dossier preparation, and lifecycle management across multiple markets
- Drive RIMS implementation and optimization (e.g., Veeva Vault RIM) to improve data integrity and regulatory efficiency
- Design regulatory roadmaps aligning processes, technology, and operating models
- Support health authority interactions, responses to queries, and regulatory communications
- Identify opportunities for process standardization, automation, and digital enablement within regulatory operations
- Engage client stakeholders to propose innovative regulatory and digital solutions
- Contribute to business development, proposals, client presentations, and regulatory thought leadership
- Stay current with changing regulatory requirements, assess impacts, and advise proactive client strategies
- Develop people through effective coaching and mentoring
- Conduct performance reviews and contribute to performance feedback
Requirements
What you’ll need- 8–12 years of hands-on experience in regulatory area with preferable experience on Veeva Vault RIMS or similar platforms
- Proven experience in regulatory affairs and RIMS implementation or management
- Strong interpersonal, written, and presentation skills
- Experience managing teams and delivering complex regulatory programs
- At managerial positions within Information Technology (IT) and/or Quality Assurance (QA) for major organizations
- Experience in managing team and solution designing
- Ideally, you’ll also have Certifications such as Regulatory Affairs Certification (RAC) or Project Management Professional (PMP)
- Experience with global regulatory submissions and lifecycle management, global audits and inspections
- Familiarity with emerging technologies in regulatory affairs, including AI/ML and automation tools
- Knowledge of IDMP compliance and structured data management for regulatory processes
- Experience in industry leading tools – Veeva vault, RimSys, Lorenz, etc.
Benefits
Comp & perks- Support, coaching and feedback from some of the most engaging colleagues around
- Opportunities to develop new skills and progress your career
- The freedom and flexibility to handle your role in a way that’s right for you
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
regulatory strategy developmentregulatory submissionsdossier preparationlifecycle managementRIMS implementationdata integrityprocess standardizationautomationdigital enablementIDMP compliance
Soft Skills
interpersonal skillswritten communicationpresentation skillscoachingmentoringteam managementperformance feedbackclient engagementinnovative solutionsthought leadership
Certifications
Regulatory Affairs Certification (RAC)Project Management Professional (PMP)