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Syneos Health

Regulatory Publishing Manager, LATAM

Syneos Health

. Create, assemble, and publish electronic submissions for global health authorities .

Posted 9/17/2026full-timeRemoteMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in creating, assembling, validating, and publishing electronic regulatory submissions while ensuring compliance with health authority guidance and industry standards. Proven ability to manage submission portfolios and collaborate effectively with cross-functional teams to drive process improvements and timely delivery.

Highest-signal resume keywords
Electronic Regulatory SubmissionsHealth Authority GuidanceSubmission Portfolio ManagementCollaboration with Regulatory LeadsProcess Improvement

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Creating Electronic SubmissionsAssembling Submission ComponentsValidating SubmissionsManaging Submission LifecyclesDocument Formatting Standards
Soft Skills
Independent WorkStakeholder CoordinationTimely Delivery
Tools & Technologies
Publishing/Content Systems
Industry Keywords
Regulatory RequirementsQuality-Driven ExecutionComplianceSubmission Readiness

About the role

Key responsibilities & impact
  • Create, assemble, and publish electronic submissions for global health authorities
  • Lead publishing activities across a portfolio
  • Maintain and manage the lifecycle of inter-related submissions with multiple concurrent submissions
  • Lead complex submission work across programs
  • Coordinate with stakeholders and project teams to ensure timely delivery of publishable content
  • Drive standards and expectations for document format
  • Ensure published output meets Vertex, industry, and health authority standards
  • Lead process improvements for accurate, quality-driven submission execution
  • Create and assemble submission components in required formats
  • Validate submissions
  • Manage portfolio views of upcoming submissions and publishing interdependencies
  • Collaborate with submission managers and regulatory leads on preparation and timelines
  • Liaise with functional source areas to ensure documents are compliant and submission-ready
  • Collaborate with regulatory document authors to resolve issues and ensure compliance with guidance and templates

Requirements

What you’ll need
  • Experience creating, assembling, validating, and publishing electronic regulatory submissions
  • Ability to work independently within publishing/content systems
  • Knowledge of health authority guidance and regulatory requirements
  • Ability to manage submission portfolios and publishing interdependencies
  • Experience collaborating with submission managers, regulatory leads, functional source areas, and regulatory document authors
  • Equivalent experience, skills, and/or education will be considered

Benefits

Comp & perks
  • Career development and progression
  • Supportive and engaged line management
  • Technical and therapeutic area training
  • Peer recognition
  • Total rewards program
  • Inclusive culture
  • Remote work arrangement (Remote (Pre-Approved))