Site Monitor Lagos Nigeria

Job Advert: Site Monitor Lagos Nigeria

Limited Duration Contract

Location: Lagos Nigeria
Experience Required: Clinical Monitoring & Clinical Research Experience (to be assessed during the interview process)

Overview

We are seeking an experienced Site Monitor to support site closure monitoring activities for ongoing clinical trials in Lagos. The successful candidate will ensure that all study closeout processes comply with regulatory requirements Good Clinical Practice (GCP) and internal quality standards. This role serves as the key liaison between the clinical trial site and the sponsor ensuring the integrity quality and completion of all site closure deliverables.

Key Responsibilities

Site Closure Monitoring

• Conduct site closure visits in accordance with study protocols regulatory requirements and SOPs.
• Verify that all study documentation investigational products and trial-related data are reconciled and archived accurately.
• Ensure all outstanding queries issues and action items are fully resolved prior to site closure.
• Confirm the completeness and proper storage of all regulatory documents and essential study records.

Quality Assurance

• Review site documentation to ensure accuracy completeness and compliance with GCP.
• Implement quality control measures to safeguard data integrity during site closure.
• Identify deviations or issues and support their timely resolution.

Regulatory Compliance

• Ensure all site closure activities meet applicable regulatory requirements including ICHGCP.
• Stay informed of changes in relevant regulations and industry best practices.

Communication & Collaboration

• Serve as the primary point of contact for site staff throughout the closure process.
• Maintain effective communication between the site sponsor and internal stakeholders.
• Provide regular progress updates to the Clinical Operations Manager regarding site closure status.

Qualifications

• Bachelors degree in Life Sciences Nursing or a related field; an advanced degree is an advantage.
• Minimum 2 years of clinical research experience preferably with handson site monitoring and/or site closure activities.
• Solid understanding of GCP ICH guidelines and regulatory expectations.
• Strong attention to detail and exceptional organizational skills.
• Excellent communication and interpersonal abilities.
• Ability to travel as required.

Key Skills

• Proficiency in CTMS and EDC systems.
• Strong analytical and problemsolving skills.
• Ability to manage multiple priorities and meet deadlines independently.

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IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.