
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
🕒 August 21
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1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
• Develop, test and execute SAS programs to produce and validate CDISC SDTM and ADaM datasets, tables, figures and listings • Review clinical database specifications, data transfer agreements/specifications, statistical analysis plan programming sections and TFL shells for medium-complexity studies • Develop and review SDTM and ADaM dataset specifications, safety-data specifications, TFL shells, patient profiles and OPS reports • Develop electronic data submission packages, including SDTM annotated CRF, define.xml and Study/Analysis Data Reviewer's Guide • Serve as programming project lead on medium-complexity studies • Distribute and oversee programming team tasks • Communicate with internal and external clients • Plan and execute delivery, manage resources and competing project priorities with line manager or mentor support • Ensure project budget and scope remain aligned • Collaborate with statisticians, sponsors, the wider study team and fellow programmers to ensure study data and outputs meet industry, regulatory submission and quality standards
• Educated to degree level or equivalent • Advanced SAS programming skills, including SAS/Macro, Proc Report and ODS • Good working knowledge of SAS/Graph and Proc SQL • Minimum 3 years of previous related experience • Computer literate and numerate • Willingness to adapt to various computer systems • Expert-level statistical programming experience • Experience providing programming leadership to projects • Statistical programming knowledge across a broad range of applications • Customer focus, delivering on commitments, relationship-building, communication and influencing, and adaptability to innovation and change
• Diverse and inclusive work environment • Supportive and cohesive teams • Accessible leadership • Opportunities for professional growth and continual learning in SAS and CDISC • Equal employment opportunities • Exceptional employee experiences
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