Data Solutions Coordinator (Regulatory Intelligence)

REDICA Systems Remote

About the role

This is a mid-level data role at REDICA Systems, a regulatory intelligence SaaS platform, fully remote and available to candidates globally. You'll monitor global regulatory developments across 150+ countries and classify them into structured data, combining regulatory science with data operations. The position focuses on accuracy, attention to detail and the ability to assess the business impact of regulatory changes for pharmaceutical, biotech and medical device companies.

What you’ll do

  • Monitor global regulatory authorities across 150+ countries to identify updates impacting Pharma, Biologics, MedTech and Animal Health sectors
  • Evaluate regulatory developments to determine industry scope and operational or strategic impact
  • Classify and structure regulatory intelligence within the platform, including industry and GxP tagging
  • Extract and organize metadata such as effective dates, consultation deadlines and enforcement timelines
  • Maintain awareness of evolving global regulatory frameworks and identify emerging trends
  • Ensure data accuracy and integrity through quality checks and KPI monitoring
  • Collaborate with internal teams to refine monitoring scope and classification logic
  • Suggest improvements to regulatory intelligence workflows and data processes

What they’re looking for

  • 4 years of experience in Regulatory Affairs, Quality Assurance, GxP or Regulatory Intelligence in Pharmaceutical, Biologics, Medical Device or Animal Health
  • Strong understanding of GxP principles and global regulatory frameworks
  • Ability to interpret regulatory language and assess practical industry impact
  • Experience analyzing regulatory updates and compliance-related materials
  • Effective communication skills for sharing intelligence insights and updates across teams
  • Demonstrated ability to make sound decisions in data operations
  • Strong attention to detail and commitment to data accuracy
  • Basic understanding of current data operations technologies and comfort adopting new tools
  • Business insight and understanding of how data decisions impact the organization

Nice to have

  • Master's degree in Regulatory Affairs, Pharmaceutics or Quality Assurance
  • Experience at top pharma companies or medical device companies
  • Knowledge of FOIA processes or government inspection data

What’s on offer

  • Full-time remote position
  • Salary not disclosed

Questions about this role

Is this role remote?

Yes, this is a fully remote position available globally.

What's the minimum experience required?

4 years of experience in Regulatory Affairs, Quality Assurance, GxP or Regulatory Intelligence within regulated industries is preferred.

What does the role pay?

Compensation is not disclosed in the posting.

Do I need a degree?

A Master's degree in Regulatory Affairs, Pharmaceutics or Quality Assurance is preferred but not required. Equivalent professional experience in regulatory affairs or quality assurance is valued.

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