Senior Clinical Programmer

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Allucent

Site WebLinkedInTous les Emplois

1001 - 5000 employés

💼 Conseil

🏥 Santé

📦 Logistique

Consulting • Healthcare • Logistics

Allucent est un partenaire de premier plan pour les petites et moyennes entreprises biotechnologiques, offrant des solutions innovantes de développement réglementaire et clinique. Avec plus de 30 ans d'expérience, Allucent se spécialise dans l'expertise thérapeutique, la pharmacologie clinique, la stratégie réglementaire, la sécurité des médicaments et les processus de pharmacovigilance nécessaires pour amener de nouvelles thérapies sur le marché. Leurs services complets répondent aux défis de la découverte précoce de médicaments jusqu'aux essais cliniques et à la surveillance post-commercialisation, soutenant divers domaines thérapeutiques tels que l'oncologie, les maladies infectieuses, la neurologie, les maladies auto-immunes et les maladies rares. L'engagement d'Allucent à encourager la science innovante aide les entreprises biotechnologiques à naviguer efficacement et efficacement dans les complexités du développement des médicaments.

Description

• 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.

🎯 Exigences

• 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)

🏖️ Avantages

• 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