
501 - 1000 employees
Founded 2012
đ„ Healthcare
đ Pharmaceuticals
đ§Ź Biotechnology
Healthcare âą Pharmaceuticals âą 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.
đ„ 7 minutes ago
đ United Kingdom, Poland â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ Manager
đ» Ghost score 10%
Where this job comes from
Posted on Veramed's careers page, not through a job board
First seen by Remote Rocketship 7 minutes ago

501 - 1000 employees
Founded 2012
đ„ Healthcare
đ Pharmaceuticals
đ§Ź Biotechnology
Healthcare âą Pharmaceuticals âą 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.
âą Support ingestion of clinical data from EDC/CTMS and vendors into Veeva CDB, Elluminate, and JReview by executing loads according to approved specifications and refresh cadence âą Execute and support file/API-based loads, including mapping, transformations, referential integrity, and controlled reprocessing âą Perform and document ingestion quality checks, automated QC/validation outputs, reconciliation results, and basic lineage/provenance âą Maintain reusable ingestion templates, mappings, QC rules, and runbooks; propose improvements to reduce manual effort âą Monitor transfers and ingestion operations, including expected-versus-received checks, timeliness/completeness checks, alert triage, escalation, scheduling, reruns, defect logging, and operational metrics âą Prepare and validate downstream exports/feeds for CDM, analytics, and programming against defined data contracts and refresh expectations âą Partner with vendors and internal stakeholders to clarify transfer specifications and acceptance criteria, troubleshoot issues, and document fixes âą Follow controlled documentation and change practices, maintaining validation/traceability evidence and audit-ready records
âą BS/BA (or equivalent) plus 5+ years in data ingestion/integration, ETL/ELT operations, or clinical data pipeline support âą Experience ideally supporting clinical data review and recurring study/vendor transfers âą Exposure to clinical data review systems such as Veeva CDB, Elluminate, and/or JReview (or comparable platforms) preferred âą Understanding of transfer specifications/data contracts, refresh cadence, incremental vs. full loads, controlled reprocessing, reconciliation, and basic lineage âą Ability to execute defined QC/validation checks and document results âą Hands-on experience with CSV, JSON, XML, and file/API-based integrations âą Familiarity with secure transfers such as SFTP/MFT concepts is a plus âą Working knowledge of SQL and Python (preferred) or similar scripting âą Ability to maintain and extend reusable ingestion components under guidance âą Experience with monitoring and operational processes, including expected-versus-received checks, alerts, reruns, incident triage, and operational metrics âą Familiarity with EDC, CTMS, and vendor feeds such as labs, eCOA/ePRO, imaging, and safety âą Strong documentation habits and ability to follow defined procedures in controlled/regulated settings âą Clear communication and collaborative working with vendors and cross-functional partners âą Detail-oriented and organized; able to manage recurring operational tasks, escalate risks, and drive issues to closure with support
âą Equal opportunities employer âą Inclusive and diverse working environment âą Working culture based on integrity, honesty, and respect âą Veramed is a B Corp accredited company committed to social and environmental performance, transparency, and accountability
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