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Junior Clinical Data Coordinator

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Onsite

Junior Clinical Data Coordinator

Mango5

Junior Clinical Data Coordinator

Skills

Google Cloud PlatformCompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Zamfara, Nigeria

Work mode:

Onsite

Published on:

20 August 2026

What they need


Are you detail-oriented with a passion for data accuracy and clinical excellence? Mango5 is looking for an experienced Junior Clinical Data Coordinator – Advanced to support global clinical trials by ensuring the highest standards of data integrity and compliance.

Role Overview:

As a Junior Clinical Data Coordinator, you will lead data consistency efforts across assigned clinical studies. You’ll ensure that all data entered is accurate, protocol-aligned, and efficiently managed across Electronic Data Capture (EDC) platforms. As the first-tier escalation point for complex data issues, your role is critical to delivering high-quality clinical outcomes.

Key Responsibilities:

  • Accurately and efficiently enter clinical data into Electronic Data Capture (EDC) systems
  • Collaborate with clinical sites and data managers to resolve data queries promptly
  • Review lab results to identify abnormalities or protocol deviations and escalate appropriately
  • Track patient visits, procedures, and follow-up schedules
  • Maintain GCP-compliant documentation of study-related communications and data
  • Communicate with patients and site staff on data status and subject compliance
  • Generate and manage Regulatory documentation for ongoing studies
  • Build and update electronic source documents as required

Requirements:

  • Matric (Grade 12) or equivalent qualification is required
  • Medical degree or Diploma strongly preferred
  • Minimum 2 years of experience in clinical data entry, data management, or administrative clinical support
  • Familiarity with clinical trial processes, EDC platforms, and data validation
  • Excellent process orientation with the ability to work across multiple systems and spreadsheets
  • Understanding of Good Clinical Practice (GCP) and clinical documentation standards
  • Strong verbal and written communication skills
  • Ability to work independently and take ownership of critical study components
  • Clear Criminal record
  • Willingness to work in USA CST hours

Working Hours:

  • 45-hour work week with rotating shifts between 15:00 – 03:00
  • Rotating working days from Monday to Sunday to ensure consistent global support
  • Dynamic holiday policy aligned to international project timelines

Remuneration Structure:

  • Basic Salary
  • Commission
  • Anniversary Bonus

Benefits:

  • Medical Insurance (after 3 months)
  • Emergency Assistance Access
  • Learning & Development support through our internal LMS portal

Be part of a dynamic team contributing to global health through precision and excellence in clinical data. Apply now and take your next step with Mango5!

If you meet the criteria but do not hear from us within 2 weeks, we will keep your profile on file for future opportunities.

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