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    • Experience in central monitoring and clinical data review is a plus.
    • Review EDC, IxRS, Laboratory and other vendors’ data and clinical listings.
    • View all PSI CRO jobs - Pretoria jobs - Clinical Data Analyst jobs in Pretoria, Gauteng
    • Salary Search: Clinical Data Reviewer salaries
    • Experience in developing protocols, desk research, clinical policy, benefit designs.
    • Sound clinical and benefit knowledge to address day-to-day as well as…
    • Review clinical data remotely and identify errors, systemic issues and trends related to data integrity, participant safety and site performance.
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    • Bachelor’s degree in a Health or Science discipline with experience in clinical research.
    • Experience working in highly diverse teams within clinical research;…
    • Salary: Market-Related, depending on experience.*.
    • Assisting with protocol/project specific regulatory issues, communication and submission, including those…
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Job Post Details

Clinical Data Reviewer - job post

PSI CRO
3.3 out of 5 stars
Pretoria, Gauteng
Full-time

Job details

Job type

  • Full-time

Location

Pretoria, Gauteng

Full job description

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 2,700 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 global yet closely-knit team with a shared commitment to developing smart and effective approaches to project monitoring. You will have the opportunity to help shape the future of risk-based monitoring at PSI and contribute to ensuring high-quality study data. As part of your role, you will remotely monitor study data, identify potential errors and trends, and flag issues related to 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
  • Ensure site 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.

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