Clinical Data Reviewer

PSI CRO; Pretoria; Hybrid; ZAR 350 000 - 550 000; Full time

Job summary

A clinical research organization in Pretoria is seeking a dedicated professional to monitor study data and ensure high quality during clinical research. You'll be responsible for identifying errors in site performance and resolving data queries. The role requires strong analytical skills, proficiency in English, and a relevant degree. This full-time position offers a hybrid working model after a trial period for successful candidates.

Qualifications

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

Responsibilities

• Review EDC IxRS Laboratory and other vendors data and clinical listings.
• Identify errors related to site performance.
• Generate follow up and resolves data queries and site issues.

Skills

Analytical mindset

Attention to detail

Full working proficiency in English

Proficiency in MS Office applications

Education

College / University degree or equivalent

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 EDC IxRS Laboratory and other vendors data and clinical listings
• Identify single errors and systematic issues related to site performance
• Generate follow up and resolves data queries and site issues
• Identify and record protocol deviations
• Assist to Central Monitoring Manager with administrative activities including managing study data documents and reports
• Ensuresite monitors receive information on site related risk & issues. Escalate findings to study teams
• Assists with root cause investigation and follow up on site performance signals identified during central monitoring review

Qualifications

• College / University degree or an equivalent combination of education training & experience
• Prior experience in Clinical Research
• Experience in central monitoring and clinical data review is a plus
• Full working proficiency in English
• Proficiency in MS Office applications
• Analytical mindset and attention to detail
• Ability to learn plan and work 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.

Remote Work: No

Employment Type: Full-time

Key Skills

Facilities Management, Banking, Content Writing, Customer Support, Fun, Airlines

Experience: years

Vacancy: 1