Regulatory Publishing Technical Consultant (Regulatory Systems)
When our values align, there's no limit to what we can achieve.
Primary Location: Mexico
11:00 AM to 8:00 PM (Mexico Time)
Regulatory Systems & Publishing Support
- Provide technical support for regulatory publishing and submission management systems.
- Troubleshoot issues related to eCTD publishing tools, document management systems, PDF creation, Microsoft Office applications, and desktop environments.
- Configure, install, test, validate, and maintain regulatory technology solutions.
- Support system validation activities, execute test scripts, and document results.
- Maintain compliance with regulatory submission standards, publishing guidelines, and industry best practices.
- Manage multiple priorities while ensuring high-quality deliverables and service levels.
Consulting & Client Engagement
- Partner with clients, regulatory teams, and software vendors to resolve technical challenges and deliver effective solutions.
- Act as a trusted advisor on publishing technologies and regulatory systems.
- Support project teams by sharing expertise and mentoring less experienced team members.
- Participate in client meetings and provide recommendations to improve efficiency and system utilization.
- Build strong relationships with internal and external stakeholders while ensuring client satisfaction.
Required Experience & Qualifications
Must-Have Experience
- 3+ years of experience in: • Regulatory Operations
- Regulatory Publishing
- eCTD Submission Management
- Regulatory Technology Support
- Regulatory Information Management (RIM)
- Experience supporting or using one or more of the following platforms: • Veeva Vault RIM
- Documentum
- EXTEDO
- Lorenz
- Calyx RIM
- Similar regulatory publishing or document management systems
- Strong understanding of: • eCTD submissions
- Regulatory publishing processes
- Global regulatory submission standards
- Submission lifecycle management
- Experience performing: • System troubleshooting
- Software testing
- Validation activities
- User support
- Advanced proficiency with: • Microsoft Office Suite
- Adobe Acrobat
- Windows operating systems
- Fluent English communication skills, both written and verbal.
Preferred Qualifications
- Bachelor's degree in Life Sciences, Technology, Computer Science, Pharmacy, Regulatory Affairs, or a related field.
- Experience writing and executing validation protocols and test scripts.
- Experience working within a CRO, pharmaceutical, biotechnology, or regulatory technology environment.
- Prior client-facing or consulting experience.
- Experience mentoring team members or acting as a subject matter expert.
Success in This Role You will be successful if you have hands-on experience with regulatory publishing technologies and enjoy solving technical challenges while working closely with clients and cross-functional teams. Candidates with backgrounds in eCTD Publishing, Regulatory Operations, Regulatory Systems, Veeva Vault RIM, Documentum, EXTEDO, or Regulatory Technology Support are strongly encouraged to apply.
What We Offer
- Opportunity to work with cutting-edge regulatory technology and publishing systems
- Exposure to global regulatory standards and best practices
- Collaborative, matrix-based environment with opportunities for mentoring and professional development
- Direct client engagement and the ability to drive meaningful business solutions
- Competitive compensation and comprehensive benefits package
Parexel is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Not included in the source posting: about the role, what you'll do.
Who can apply
The employer didn't state any visa, work authorization, citizenship or clearance requirements in this posting. Confirm with the employer before applying.
Read automatically from the employer's posting text. Always confirm with the employer — requirements can change after a job is published.