Clinical Data Reviewer

PSI CRO; Pretoria; On-site; ZAR 350,000 - 600,000; Full time

Job summary

Join a dynamic global organization committed to quality and excellence in project monitoring. As part of a close-knit team, you will contribute to shaping risk-based monitoring strategies and ensuring high-quality study data. Ideal candidates possess a college degree and experience in clinical research, with strong analytical skills and proficiency in data review.

Benefits

Professional development opportunities

Qualifications

• Prior experience in Clinical Research.
• Experience in central monitoring and data review is a plus.
• Ability to learn, plan, and work effectively in a dynamic team environment.

Responsibilities

• Reviewing data from EDC, IxRS, Laboratory, and other vendors.
• Identifying errors and systematic issues related to site performance.
• Supporting root cause investigations on site performance.

Skills

Analytical mindset

Attention to detail

Proficiency in English

Education

College/University degree or equivalent education, training, and experience

Tools

MS Office applications

Job description

Company Description

We are a company that cares – for our staff, clients, partners, and the quality of our work. Founded in 1995, we are a dynamic, global organization with over 2,700 dedicated individuals. We work at the forefront of medical science, changing lives and bringing new medicines to those in need.

Job Description

You will join a close-knit team passionate about developing smart, effective project monitoring strategies. Your role will be to help shape the future of risk-based monitoring at PSI and ensure high-quality study data. This involves remote data monitoring, error identification, and addressing site performance issues.

Hybrid position after the trial period.

Your responsibilities include:

• Reviewing data from EDC, IxRS, Laboratory, and other vendors
• Identifying errors and systematic issues related to site performance
• Generating, following up, and resolving data queries and site issues
• Recording protocol deviations
• Assisting the Central Monitoring Manager with administrative tasks, including managing study data, documents, and reports
• Ensuring site monitors receive information on site-related risks and issues, and escalating findings to study teams
• Supporting root cause investigations and follow-up on site performance signals identified during central monitoring

Qualifications:

• College/University degree or equivalent education, training, and experience
• Prior experience in Clinical Research
• Experience in central monitoring and data review is a plus
• Proficiency in English
• 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

Take your career to the next level by joining a company that invests in its people’s professional development and success.