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Senior Clinical Data Analyst (US)

King of Prussia, United States

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 clinical data and analytics skills and a passion for delivery excellence, to help drive customer success and broad adoption of the CluePoints solution.

 

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 lead the communication of results to customers (both written report and oral presentation) 

  • Actively participate in the continuous improvement and development of our product solutions, operational processes and best practices

  • Provide consultation and related operational support to customers as needed, with the help of Project Coordinator

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

  • Provide mentoring to other Data Analysts

  • Support and participate in developing and improving training material used both internally and externally

  • Provide both on-site and off-site training to customers

  • 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 progromming languages, and preferably with statistical programming (SAS, R …) 

  • Experience with and understanding of clinical trials and clinical data

  • Demonstrated strong aptitude for data analytics, 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 CDISC databases is a plus  

 

Qualifications Needed

  • College degree, preferably in a scientific or technical discipline

  • 5+ years of experience in a clinical research environment

  • Knowledge of industry regulatory and clinical data standards including 21 CFR Part 11, ICH E6 (GCP), CDISC standards, MedDRA, WHODRUG, etc.

 

How to Apply 

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