Senior Clinical Programmer

🕒 Junho 26

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Allucent

SiteLinkedInTodas as Vagas

1001 - 5000 funcionários

💼 Consultoria

🏥 Saúde

📦 Logística

Consulting • Healthcare • Logistics

A Allucent é um parceiro de referência para empresas de biotech de pequeno e médio porte, oferecendo soluções inovadoras em assuntos regulatórios e desenvolvimento clínico. Com mais de 30 anos de experiência, a Allucent é especializada em expertise terapêutica, farmacologia clínica, estratégia regulatória, segurança de medicamentos e nos processos de farmacovigilância necessários para levar novas terapias ao mercado. Seus serviços abrangentes abordam desafios desde a descoberta de fármacos em fases iniciais até os ensaios clínicos e a vigilância pós-comercialização, apoiando diversas áreas terapêuticas, como oncologia, doenças infecciosas, neurologia, doenças autoimunes e doenças raras. O compromisso da Allucent em fomentar ciência de ponta ajuda as empresas de biotech a navegar pelas complexidades do desenvolvimento de medicamentos de forma eficiente e eficaz.

Descrição

• Lead clinical programming activities across assigned studies, ensuring project timelines, budgets, deliverables, and resource needs are effectively managed while proactively identifying and escalating risks or change orders. • Design, build, validate, and maintain clinical databases, electronic edit checks, data listings, and data visualization tools to support high-quality data collection, review, and regulatory compliance. • Collaborate cross-functionally with Data Management, Project Management, Biostatistics, and study teams to develop study documentation, clarify technical specifications, and deliver programming solutions that meet project objectives. • Champion industry standards and quality, applying CDISC conventions (CDASH, SDTM, TAUGs), validation principles, and programming best practices to ensure consistent, compliant, and inspection-ready deliverables. • Drive innovation and continuous improvement by leading process enhancements, developing global programming standards and libraries, implementing data analytics and visualization tools, and supporting departmental initiatives.

🎯 Requisitos

• Life science, healthcare, Computer Science and/or related field degree • Minimum 5 years of experience in drug development and/or clinical research • Good understanding and hands-on experiences of CDISC standards (i.e. CDASH, TAUGs and SDTM models) • Expert with electronic data capture (EDC) software systems and other tools for managing clinical studies • Expert in technical data management practices (developing programs, validation plans, testing, and documentation)

🏖️ Benefícios

• Comprehensive benefits package per location • Competitive salaries per location • Departmental Study/Training Budget for furthering professional development • Flexible Working hours (within reason) • Opportunity for remote/hybrid* working depending on location • Leadership and mentoring opportunities • Participation in our enriching Buddy Program as a new or existing employee • Internal growth opportunities and career progression • Financially rewarding internal employee referral program • Access to online soft-skills and technical training via internal platforms • Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects • Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees