Senior/Principal Statistical Programmer/Analyst Consultant (Cardiovascular, Renal)-Remote -Outside IR35

ClinchoiceRemotosenior

En corto

▸Programador estadístico senior con enfoque en estudios cardiovasculares, renales y metabólicos.
▸Trabaja remotamente, genera y valida estándares CDISC (SDTM, ADaM, TLF) bajo supervisión de líder técnico.
▸Contrato fuera de IR35 con estabilidad de CRO global y exposición directa a sponsor.

Good communication and stakeholder management skills

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¿Qué piden?

✓Experiencia sólida en SAS en entornos farmacéuticos/CRO
✓Experiencia directa en estudios CVRM (Cardiovascular, Renal & Metabolism)
✓Generación y validación de SDTM, ADaM y TLF
✓Conocimiento profundo de estándares CDISC
✓Capacidad para trabajar de forma independiente con múltiples prioridades
✓Experiencia en presentaciones regulatorias es deseable

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SASSDTMADaMTLFCDISCClinical Trial ProcessesRegulatory SubmissionsProgrammingData StandardsProject Delivery

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Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients in . ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. Main Job Tasks and Responsibilities: The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Key Requirement: • Strong SAS programming experience within the pharmaceutical/CRO industry • Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies • Experience in generating and validating SDTM, ADaM, and TLFs • Good understanding of CDISC standards and clinical trial processes • Ability to work independently and manage multiple priorities in a fast-paced environment • Experience supporting regulatory submissions is preferred • Strong communication and stakeholder management skills Responsibilities: <li style="fon

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