Clinical Research QA Specialist
Job Description
A reputable healthcare organization in Abuja is seeking a qualified Clinical Research QA Specialist to support and strengthen clinical trial quality systems. The role focuses on ensuring that all clinical studies are conducted in strict compliance with approved protocols, Good Clinical Practice (GCP), and applicable regulatory requirements, while maintaining data integrity and participant safety.
Location: Abuja (FCT)
Employment Type: Full-time
Reports To: Director of Clinical Operations
Salary: ₦300,000 – ₦400,000 per month
Application Deadline: 12th March, 2026
Key Responsibilities
- Conduct site monitoring visits to ensure compliance with study protocols and regulatory standards
- Perform source data verification (SDV) and review trial documentation for accuracy and completeness
- Monitor protocol adherence and manage deviations in line with regulatory guidelines
- Oversee Serious Adverse Event (SAE) reporting and safety compliance processes
- Provide training and guidance to site staff on GCP and study-specific procedures
- Support multi-site trial coordination and quality oversight activities
- Prepare monitoring reports and escalate compliance issues where necessary
Requirements
- Proven experience in clinical trial monitoring or clinical quality assurance
- Strong knowledge of Good Clinical Practice (GCP) and regulatory compliance standards
- Experience working on multi-site clinical trials is preferred
- Excellent documentation review and analytical skills
- Strong communication and stakeholder coordination abilities
- High level of attention to detail and commitment to data integrity
How to Apply
Interested and qualified candidates should send their CV using Clinical Research QA Specialist as the subject of the email.
