Clinical Data Analyst: Data Integrity & Insights

MaximaTek; Town of Texas (WI); Sur place; USD 65 000 - 90 000; Plein temps

Résumé du poste

MaximaTek is seeking a detail-oriented Clinical Data Analyst to support collection, management, cleaning, and reporting of clinical trial and healthcare data. You will bridge clinical operations, data management, and biostatistics to ensure data integrity and protocol compliance across studies.

The role involves validating data in CDMS/EDC, performing exploratory analyses, and producing dashboards using SQL, SAS, R, or Python.

Qualifications

• Bachelor’s or Master’s in Health Informatics, Biostatistics, Data Science, Life Sciences, or related quantitative field (Required).
• 0–5 years of experience in clinical data management, clinical analytics, healthcare research, or CRO environments.
• Strong analytical and data-driven problem-solving skills.
• Proficiency in SQL and database query writing.
• Hands-on experience with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, REDCap, Oracle InForm).
• Knowledge of clinical trial processes, medical terminology, and GCP standards.

Responsabilités

• Review, clean, and validate clinical trial data in CDMS/EDC.
• Identify data discrepancies, issue queries, and track resolutions.
• Participate in UAT, eCRF design, and data validation checks.
• Perform exploratory data analysis and generate routine reports, dashboards, and visualizations.
• Ensure data collection adheres to GCP, CDISC SDTM/ADaM, HIPAA, FDA/EMA.

Connaissances

SQL

Data Cleaning

Analytical Thinking

Communication

EDC Systems

Formation

Bachelor’s or Master’s in Health Informatics/Biostatistics/Data Science/Life Sciences

Outils

Medidata Rave

REDCap

Tableau

Power BI

SAS/Python/R

Description du poste

MaximaTek is seeking a detail-oriented Clinical Data Analyst to support collection, management, cleaning, and reporting of clinical trial and healthcare data. You will bridge clinical operations, data management, and biostatistics to ensure data integrity and protocol compliance across studies.

The role involves validating data in CDMS/EDC, performing exploratory analyses, and producing dashboards using SQL, SAS, R, or Python.