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PSI CRO

200 open roles · Process Improvement

Clinical Data Reviewer

Full-time
Posted 4 weeks ago
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Where you can work

Unspecified

Locations named in the listing

  • Pretoria, Gauteng, South Africa
View location wording from the posting
Pretoria, GP, South Africa

Role overview

Extracted from the posting. Read the employer’s full description below.

What they are looking for

  • 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
Show all 7 items
  • Analytical mindset and attention to detail
  • Ability to learn, plan and work in a dynamic team environment

Employer 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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Source: SmartRecruiters