NexGen Research Ltd

Clinical Research Coordinator

NexGen Research Ltd

Research, Teaching & Training

Today
Easy apply New
Enugu Full Time Healthcare NGN 250,000 - 400,000

Job summary

NexGen Research is seeking a detail-oriented Clinical Research Coordinator to support global clinical trial operations remotely. Responsibilities include regulatory document management, data entry, study tracking, and quality assurance activities. Strong computer skills, excellent English communication, and availability during U.S. Eastern time.

Min Qualification: Degree Experience Level: Entry level Experience Length: 1 year Language Requirement: English Working Hours: Full Time - 8 to 5 Applicant Location: Enugu, Nigeria

Job descriptions & requirements

Responsibilities:

  • Assist with clinical trial regulatory document management
  • Prepare and maintain electronic regulatory binders
  • Enter and review study data in Electronic Data Capture (EDC) systems
  • Track study documentation and investigator training records
  • Support subject recruitment and pre-screening activities
  • Assist with adverse event and protocol deviation documentation
  • Review medical records and source documents for completeness
  • Prepare reports, logs, trackers, and study-related correspondence
  • Schedule investigator meetings and training sessions
  • Support quality assurance and compliance activities
  • Coordinate with investigators, sponsors, and CROs globally


Requirements:

  • Bachelor's degree or higher in: Medicine, Nursing, Pharmacy, Medical Laboratory Science, Public Health, Biological Sciences, and Life Sciences or related field
  • Excellent written and spoken English
  • Strong computer skills and proficiency with Microsoft Office
  • Reliable internet connection and personal computer
  • Close attention to detail and ability to meet deadlines
  • Ability to work during U.S. business hours


Preferred Qualifications:

  • Prior clinical research experience
  • GCP certification
  • Experience with EDC systems
  • Experience with regulatory documentation
  • Healthcare or medical records experience


Benefits:

  • Comprehensive clinical research training
  • Exposure to global clinical trial operations
  • Career development opportunities
  • Mentorship from experienced investigators and research professionals
  • Competitive compensation
  • Long-term growth potential within a rapidly expanding research organization

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