Clinical Trial Manager at Avocado Virtual Solutions (AVS)

Clinical Trial Manager at Avocado Virtual Solutions (AVS) - April 7, 2026

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Clinical Trial Manager at Avocado Virtual Solutions (AVS) ⏲ Apr 7, 2026, 9:25 PM ⋕ View all Medical & Health jobs

Avocado Virtual Solutions (AVS) is a professional recruitment agency and business support service dedicated to helping entrepreneurs, small businesses, and busy professionals streamline their operations. We specialize in administrative support, customer service, social media management, recruitment assistance with onboarding, and business/company branding. Our mission is to help clients save time, enhance productivity, and build strong, recognizable brands while they focus on growing their businesses.

We are recruiting to fill the position below:

Job Title: Clinical Trial Manager

Location: Abuja (FCT) 

Employment Type: Full-time

Position Summary

The Clinical Trial Manager (CTM) is responsible for the end to end operational management of clinical trials conducted by Afro REACH CRO. Based in Abuja, Nigeria, the CTM will oversee the planning, execution, monitoring, and close out of clinical studies, ensuring they are delivered on time, within budget, and in full compliance with ICH GCP, regulatory requirements, and sponsor expectations.

This role serves as the primary operational liaison between sponsors, investigators, study sites, vendors, and internal project teams.

Key Responsibilities

Lead the operational planning and execution of clinical trials from study start up through close out

Develop and maintain clinical trial plans, timelines, and tracking tools

Ensure trials are conducted in accordance with study protocols, SOPs, ICH GCP, and applicable regulations

Coordinate site selection, initiation, monitoring, and close out activities

Oversee protocol deviations, corrective and preventive actions (CAPAs), and risk mitigation strategies

Ensure compliance with regulatory and ethical bodies

Support regulatory submissions, approvals, and ongoing communications with authorities

Ensure informed consent processes and participant protections are rigorously upheld

Lead study meetings, status calls, and investigator meetings

Provide regular progress reports, risk assessments, and issue escalation to leadership

Ensure accurate and timely trial documentation, including TMF completeness

Support audit and inspection readiness and responses

Promote a culture of continuous quality improvement and operational excellence

Supervise Clinical Research Associates (CRAs) and other study team members

Provide training, mentorship, and performance oversight for assigned staff

Manage third party vendors (e.g., laboratories, imaging providers, logistics vendors)

Facilitate cross functional collaboration with data management, pharmacovigilance, and quality teams

Act as the primary point of

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