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Specialized clinical tools plus metro location and mid-level experience create moderate applicant competition.
Clinical data programming requires domain-specific tools and standards, making cross-industry transfer difficult.
Explicit 3-5 years plus mandatory Elluminate/reporting skills and clinical standards increase shortlisting rigor.
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Design and develop clinical data cleaning and reporting solutions using Elluminate and other tools to support data quality and study monitoring.
Collaborate with cross-functional teams to create and automate business rules and reusable check libraries for data validation across studies.
Enhance or create reporting tools and listings for clinical trial data review, ensuring compliance with SOPs and operational excellence.
Bachelor's degree in computer science, statistics, biostatistics, mathematics, biology, or related health field or equivalent experience.
3-5 years' experience programming listings and visualizations with Veeva CDB, JReview, and Elluminate, particularly hands-on report development in Elluminate.
Proficiency in one or more programming languages: CQL, SQL, SAS, R, Python.
Knowledge of clinical trial terminology, drug development process, regulatory requirements, and preferred familiarity with CDISC and SDTM standards.
Experienced in clinical data programming within fast-paced environments handling complex trial data and data cleaning processes.
Strong collaborator capable of working with data engineers, configuration specialists, and cross-functional teams to develop automated data quality checks.
Technically proficient with clinical database systems (e.g., Metadata Rave, Veeva, Inform) and capable of independently delivering high-quality, compliant data cleaning reports.