
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.
🔥 7 minutes ago
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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.
• Generate Data Management listings and support protocol deviation reporting • Develop or quality control SDTM datasets for individual studies and pooled analyses • Produce and review Define.xml and SDRG documentation • Support Dry Runs, Interim Analyses, IDMC reviews, DSURs and Final Analyses • Ensure deliverables comply with sponsor SOPs, processes and quality standards • Collaborate with cross-functional teams and communicate project risks or issues as needed
• Strong SAS programming experience within clinical research • Good knowledge of CDISC SDTM standards (v3.3 and/or v3.4) • Experience developing or QC'ing SDTM datasets • Familiarity with Pinnacle 21 or similar validation tools • Excellent communication and stakeholder management skills
• Opportunity to gain exposure to SDTM programming • Professional growth and development • Collaborative team environment • Work closely with a leading sponsor • Equal opportunities employer • Inclusive and sustainable workplace culture
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