
501 - 1000 employees
Founded 2012
🏥 Healthcare
💊 Pharmaceuticals
🧬 Biotechnology
Healthcare • Pharmaceuticals • Biotechnology
Veramed is a biometrics-focused contract research organization (CRO) that provides data management, biostatistics, programming, evidence & value generation, and standards/AI services to pharmaceutical and biotechnology clients. The company offers end-to-end biometrics support, Functional Service Provider (FSP) and project-based delivery models, regulatory submission-ready data, advanced automation and AI (Veramed. ai), CDISC compliance, and data visualization to minimize submission issues and audit findings. Veramed positions itself as a trusted partner for biotech and pharma, emphasizing operational governance, scalability, and a people-first culture.
🔥 0 minutes ago
Where this job comes from
Posted on Veramed's careers page, not through a job board
First seen by Remote Rocketship 0 minutes ago

501 - 1000 employees
Founded 2012
🏥 Healthcare
💊 Pharmaceuticals
🧬 Biotechnology
Healthcare • Pharmaceuticals • Biotechnology
Veramed is a biometrics-focused contract research organization (CRO) that provides data management, biostatistics, programming, evidence & value generation, and standards/AI services to pharmaceutical and biotechnology clients. The company offers end-to-end biometrics support, Functional Service Provider (FSP) and project-based delivery models, regulatory submission-ready data, advanced automation and AI (Veramed. ai), CDISC compliance, and data visualization to minimize submission issues and audit findings. Veramed positions itself as a trusted partner for biotech and pharma, emphasizing operational governance, scalability, and a people-first culture.
• Configure study-level clinical data extraction, transformation, and transfer outputs across multiple data sources according to Data Transfer Agreements and technical specifications • Partner with internal and external stakeholders, including Data Engineers, to deliver required data formats and frequencies with high quality and on time • Support implementation of sponsor-defined data transfer standards and specifications • Provide input to documentation and training materials • Perform or coordinate quality review of configuration and deliverables • Oversee and review vendor-performed work as needed • Manage and train other team members • Complete other assigned duties within timelines
• Experience with EDC build/data management or EDC extraction/configuration • Strong understanding of clinical data flow (CDMS, vendor devices, CDR) • Familiarity with data cleaning tools such as Veeva CDB, J Review, and Elluminate • Strong clinical trial terminology and data transfer specification knowledge • Understanding of SDTM • Data/integration experience with XMLs, APIs, and MDR preferred • ETL/ELT experience • Programming experience in one or more of SQL, SAS, R, or Python preferred • R Shiny/Python app development experience • Proficiency with Microsoft Office • Independent and collaborative problem-solving • Ability to prioritize and work in a fast-paced environment • Strong project management skills, initiative, deadline management, attention to detail, organization, and time management • Quick learner comfortable with new technologies and systems
• Equal opportunities employer • Inclusive and diverse working culture • B Corp accredited company focused on social and environmental performance, transparency, and accountability
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