Clinical Data Reviewer

PSI CRO·Pretoria, GP, South Africa

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About the role

Hybrid Clinical Data Reviewer role in Pretoria after a trial period. The position reviews clinical data remotely, identifies data integrity and site-performance issues, manages queries, supports central and risk-based monitoring, maintains review tools, investigates signals and contributes to inspection readiness. A bachelor’s degree, at least one year of clinical research industry experience, English at CEFR B2 or above and MS Office proficiency are required; clinical monitoring experience is advantageous.

Key requirements

• Bachelor’s degree
• At least 1 year of relevant experience
• Required skills: Clinical research industry experience, Reviewing clinical data, Identifying data errors, systemic issues and trends, Data query and site issue management, Identifying potential protocol deviations, Developing and maintaining central data review tools, templates and tracking materials, Risk-based and central monitoring support, Central monitoring signal review, Root cause investigation, Inspection readiness, eTMF quality control, MS Office applications, Analytical mindset, Attention to detail, English proficiency at CEFR B2 level or above, Ability to learn, plan and work effectively in a dynamic team environment
• Required language: English

Opportunity details

• Workplace: Hybrid
• Posted: Oct 23, 2026
• Original advert language: English

Full vacancy

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Employer’s role description

Job title: Clinical Data Reviewer

Location: Pretoria, GP, South Africa

Employment type: Full-time

Workplace type: Hybrid

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

You will join a widespread, yet closely-knit team with the same mentality and desire to develop smart and intelligent approach to project monitoring. You will help to shape the future of effective risk-based monitoring at PSI and ensure higher quality of study data. You will spend time monitoring study data remotely, identifying errors and issues with site performance.

Hybrid position after trial period.

You will:

Review clinical data remotely and identify errors, systemic issues and trends related to data integrity, participant safety and site performance
Generate, follow up and resolve data queries and site issues, and identify potential protocol deviations
Develop and maintain study-specific Central Data Review tools, templates and tracking materials
Support the setup and management of risk-based and central monitoring tools and activities
Assist with central monitoring signal review, root cause investigation and follow-up
Support the Central Monitoring Manager with study data, documents and reports
Contribute to inspection readiness, including eTMF QC and study archive activities

Qualifications

Bachelor’s degree
At least 1 year of experience in the Clinical Research Industry
Clinical Monitoring experience is an advantage
English proficiency at CEFR B2 level or above
Proficiency in MS Office applications
Analytical mindset and attention to detail
Ability to learn, plan and work effectively in a dynamic team environment

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.