Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
November 27
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
• Work as a Clinical Programmer responsible for data review and trial management deliverables across all compounds and trials. • Liaise with Clinical Data Management to understand end-user needs. • Create software systems to generate displays of clinical study data and metrics reports. • Document archives of software and deliverables and create work instructions. • Provide time and resource estimates for project planning.
• Bachelor’s degree in computer science, Statistics, Mathematics, Life Sciences or other relevant scientific fields. • Minimum of 5 years of experience in developing software in a clinical trial environment using SQL, including at least 3 years of clinical programming experience. • Skilled in programming in a relational database setting with SQL and/or T-SQL or ETL. • Experience with data reporting tools in a clinical trial setting. • Experience in the Biotechnology, Pharmaceutical, or Life Sciences industries (Clinical Research Organization - CRO or Clinical Trial regulated environment preferred). • Experience with the eClinical Solutions elluminate platform a plus; experience with Qlik Sense a plus. • Preferred additional external data transfer experience in: - Creating external data transfer specifications, ensuring external clinical trial data are compatible with the clinical database to support data integration, analysis and reporting. • Experience in planning, set-up, and acquisition of external clinical data at the study level. • Liaising with and reviewing work delivered by external partners (e.g. laboratories, eCOA providers, technology providers, etc.) • Knowledge of some additional programming languages (e.g.: SAS, PL/SQL, R, Python, Java, …) a plus. • Ability to balance and prioritize multiple assignments and respond quickly to ad hoc requests. • Familiarity with CDISC standards, including CDASH and SDTM. • Working knowledge of Microsoft products: Outlook, Word, Excel, Teams. • Excellent verbal and written communication skills. • Strong English language written and verbal communication skills.
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