Position: Associate

Job type: Full-time

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Job content

CluePoints is a fast-growing company and the premier provider of Risk-Based Monitoring and Data Quality Oversight solutions to Bio-Pharmaceutical and Medical Device organizations. Our products utilize advanced statistical algorithms to determine the quality of clinical trial data both during and following study execution. The value of CluePoints lies in its powerful and timely ability to identify anomalous data and site errors allowing highly efficient site monitoring and a significant reduction in overall regulatory submission risk. CluePoints is seeking outstanding candidates with strong clinical data and analytics skills and a passion for delivery excellence, to help drive customer success and broad adoption of the CluePoints solution.

Cluepoints has been awarded as Scale-up of the year 2019 by Ernst & Young.

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 (strong preference for SAS)
  • 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

  • University degree in Data Science or equivalent
  • 0-2 years of experience in a clinical research environment

Top Reasons to Work with Us

  • A challenging and rewarding job in an ambitious scale-up
  • Work for a fast-growing, multi-disciplinary and international team
  • Competitive salary package
  • Geek & Startup atmosphere
  • Flexible working hours and homeworking
  • Flat hierarchy
  • We offer some perks: free drinks, cookies, fruits, video games, etc…

The role will be permanently based at our Belgium office. We will strictly only consider applications from candidates that are residents and/or hold a valid work permit for the location they apply for.

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Deadline: 31-12-2025

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