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    • You will help to shape the future of effective risk-based monitoring at PSI and ensure higher quality of study data.
    • Hybrid position after trial period.
    • View all PSI CRO jobs - Pretoria jobs - Clinical Data Analyst jobs in Pretoria, Gauteng
    • Salary Search: Clinical Data Reviewer salaries
    • Centurion, South Africa | Full time | Hybrid | R1538302.
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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 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.

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