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Junior Clinical Data Analyst

Mont-Saint-Guibert, Belgium

CluePoints is an innovative, fast-growing company and the premier provider of Risk-Based Monitoring and Data Quality Oversight solutions to clinical research organizations.  Our products enable both risk planning and operational risk monitoring, and utilize advanced statistical algorithms to determine the quality of clinical trial data both during and following study execution.  CluePoints is seeking outstanding candidates with strong data analytics aptitude and a passion for delivery excellence, to help drive customer success and broad adoption of the CluePoints solution. 

Please apply only if you hold a valid work permit or if you are a national of the Member States of the European Economic Area.


Responsibilities 

  • Perform the technical configuration of the CluePoints solution for clinical studies based on customer requirements

  • Perform analyses using the CluePoints Central Monitoring Platform – diagnosing and explaining anomalies identified in the clinical study data

  • Summarize findings and support the communication of results to customers (both written report and oral presentation) 

  • Participate in the continuous improvement and development of our product solutions and operational processes

  • Provide consultation and related operational support to customers as needed, with the help of more senior Data Analysts and/or the CluePoints Project Lead

  • Ensure that appropriate documentation is produced and maintained for each study Lead

  • Assist Business Development and Quality Assurance teams in responding to client questions and requests (e.g., RFP responses, audits, etc.)

 

Skills Needed 

 

  • Experience with one or more programming languages, and preferably with statistical programming (SAS, R …) 

  • Aptitude for data analytics

  • Aptitude for mathematical and statistical concepts   

  • Excellent English oral and written communication skills 

  • Experience and ability to work well in a team environment

  • Ability to thrive in a fast-moving environment, under time and resource constraints

  • High degree of accuracy and attention to detail 

  • Experience with and understanding of clinical trials and clinical data is a plus

  • Experience with CDISC databases is a plus  

 

Qualifications Needed 

 

  • College degree, preferably in a scientific or technical discipline

  • 0 to 2+ years of experience in a clinical research environment.


How to Apply 

Please simply click the button on this page!