Clinical Programmer

March 7

Apply Now

Receive Emails with Similar Jobs

Parexel

WebsiteLinkedInAll Job Openings

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

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

📋 Description

• Program simple to complex data review listings, exception reports, QTL/KRIs, metrics reports and visualizations in a fast-paced environment for clinical trial data review and management purposes. • Liaise with Clinical Data Management and/or cross functional staff to understand the needs of the end users of the listings, reports, and metrics. • Contribute to the development of software systems and related infrastructure to generate displays of clinical study data and metrics reports that are efficient and user-friendly. • Create and document archives of software and deliverables. • Create any Work Instructions process and training documents needed related to clinical programming and the required deliverables. • Provide time and resource estimates for project planning as well as accurately record time spent on multiple deliverables.

🎯 Requirements

• 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.