Research Associate (CRA 1) at Avocado Virtual Solutions (AVS)

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: Research Associate (CRA 1)

Location: Abuja (FCT)
Employment Type: Full-time
Engagement Type: Retainer → Full Study Engagement

Job Summary

• We are seeking an experienced Clinical Research Associate (CRA) to support clinical trial monitoring, site readiness, and regulatory compliance for upcoming studies.
• The role will initially operate on a retainer/part-time basis during study preparation, transitioning to full engagement once clinical studies are activated.

Key Responsibilities

• Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements
• Conduct Site Qualification Visits (SQV), Site Initiation Visits (SIV), Monitoring Visits (IMV), and Close-Out Visits (COV)
• Perform Source Data Verification (SDV) and ensure data accuracy and integrity
• Maintain Trial Master File (TMF / eTMF) documentation to ensure inspection readiness
• Track protocol deviations, adverse events, and study-related issues
• Support investigator training and site readiness activities
• Collaborate with investigators, site coordinators, and clinical operations teams
• Prepare monitoring reports and follow-up documentation

Requirements

• Degree in Health Sciences, Medicine, Pharmacy, Nursing, or related field
• 2–4 years experience in clinical research or clinical trial monitoring
• Strong understanding of ICH-GCP guidelines and clinical trial processes
• Experience with site monitoring and regulatory documentation
• Familiarity with EDC systems and clinical documentation management
• Strong organizational and communication skills
• Ability to manage multiple sites and timelines

Preferred Experience:

• Prior experience supporting multi-site clinical trials
• Experience working with CROs, sponsors, or research institutions
• Familiarity with TMF/eTMF systems and clinical trial management tools

Engagement Structure:

• This role will begin with a retainer arrangement during study preparation, allowing flexibility for candidates currently engaged in other roles. Full engagement and compensation will apply upon study activation.

Application Closing Date
27th March, 2026. 

How to Apply
Interested and qualified candidates should send their CV to: avsabujahr@gmail.com using the Job Title as the subject of the email.‎