Data Solutions Coordinator (Reg Intel) — LATAM (Fully Remote)

Redica Systems

United States

Remote

USD 90,000 - 130,000

Full time

14 days+

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Job summary

Redica Systems is the Intelligence Cloud for life sciences, transforming regulatory complexity into connected, proactive intelligence. Their platform helps leading pharmaceutical and MedTech companies stay inspection-ready, manage supplier risk, and comply with global regulations in a fast-paced, high-growth environment.

We are seeking a Regulatory Affairs professional to monitor developments across 150+ countries, assess impact, and ensure accurate structured data entry.

Qualifications

  • 4+ years in Regulatory Affairs, Quality Assurance, GxP, or Regulatory Intelligence preferred.
  • Strong GxP knowledge, analytical judgment, and attention to detail required.

Responsibilities

  • Monitor global regulatory developments across 150+ countries and identify key updates.
  • Assess operational and strategic impact, determine industry scope, and ensure accurate structured data entry.
  • Communicate regulatory insights clearly and make timely data decisions.
  • Optimize workflows while using current data technologies and business insight.

Skills

Regulatory affairs
GxP knowledge
Analytical skills
Attention to detail

Job description

  • Monitor global regulatory developments across 150+ countries and identify key updates.
  • Assess operational and strategic impact, determine industry scope, and ensure accurate structured data entry.
About You:
  • Communicate regulatory insights clearly and make timely data decisions.
  • Optimize workflows while using current data technologies and business insight.
Qualifications:
  • 4+ years in Regulatory Affairs, Quality Assurance, GxP, or Regulatory Intelligence preferred.
  • Strong GxP knowledge, analytical judgment, and attention to detail required.

Redica Systems is the Intelligence Cloud for life sciences, transforming regulatory complexity into connected, proactive intelligence. Their platform helps leading pharmaceutical and MedTech companies stay inspection-ready, manage supplier risk, and comply with global regulations in a fast-paced, high-growth environment.

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