Job title : Quality Assurance Specialist
Job Location : Abuja Deadline : July 20, 2025 Quick Recommended Links
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Job Description
The Quality Assurance Specialist will conduct comprehensive quality assurance reviews in support of Afro-REACH Research Organization's clinical teams.This full-time position partners and collaborates with core members of the clinical trial teams from the sponsor and across research staff at site level to address findings, provide solutions for improvement, and ensure compliance within their area of expertise.The Quality Assurance Specialist will oversee audits and inspections and work cross-functionally to support continuous quality enhancement across ARO.Responsibilities
Travel to sponsor sites to QA reviews of clinical trials and processes for adherence to SOPs, policies, and NHREC and NAFDAC guidelinesPrepare reports and discuss non-compliance and quality findings with sponsors and within ARO to identify solutions and action plansProvide guidance and root-cause analysis to mitigate identified challenges and gaps in processesWork closely with clinical teams and Principal Investigator as needed to identify gaps and ensure continuous process improvementAssist in preparing for inspections by sponsors and regulatory agencies and participate in on site regulatory inspections as appropriateImplements quality management plans including risk identification and assessment through data review and quality control processesProvides consultation and corrective action plans in a timely manner and identifies preventative actions for site staff and clinical trial operations.Provides guidance on relevant updates to assist with the improvement and updates in relevant SOPs, policies, and training as neededConducts Quality Assurance training for employees and new hires when neededConducts review of training records and identified SOPs to ensure assigned sites are maintaining compliance with training curriculumStay up to date on relevant clinical trial requirements, NAFDAC, NHREC, GCP, ICH, and other relevant guidelines within Sub-Saharan Africa and other regions relevant for AROIdentify and escalate significant compliance issues as according to SOPsIdentify training gaps and ensure periodic training for ARO employeesAssist with quality incident and compliance investigations as required.Qualifications
Bachelor's Degree or equivalent related experienceStrong working knowledge of medical terminology, SOPs, International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Food and Drug Administration (FDA), applicable regulatory requirements, and quality management processes3-5 years prior work experience in a clinical quality, clinical compliance, or clinical auditing roleDirect experience in the conduct and reporting of internal and external audits preferredExcellent interpersonal, verbal, and written communication skillsClient and patient-focused approachThrives in a fast-paced environment with the ability to work independently, be proactive, and have a nimble approach with respect to day-to-day activitiesAbility to multi-task and prioritize workload with attention to detail and strong organizational skillsAbility to work effectively with cross-functional teams to foster teamwork within the group as well as across AROProficient in Microsoft Office programs such as MS Word, Outlook, Excel, PowerPoint, SharePoint, and Teams.Maintains a strong level of integrity and good judgement at all timesExperience of inspection managementFundamental knowledge of in-country and international regulatory standards and guidelines for the conduct of clinical trialsKnowledge of data integrity controls and systems quality for clinical areaStrong analytical skills and report writing skillsAbility to demonstrate tact as a representative of the CQA DepartmentMust have professional communications skills, strong independent time management skills and the ability to manage multiple projects concurrentlyAbility to Travel (approximately 25%)Preferred Qualifications :
Experience preparing for, participating in, and subsequent response to health authority GCP inspections / partner audits also preferredClinical Research or Quality Certification preferred.