Allucent

Allucent

Programmeur Clinique Principal I/ Sr. Clinical Programmer I

Montreal, Quebec, Canada · Principal

Sponsorship not specifiedDetected 21 days ago
TypeScriptData AnalysisData VisualizationNLPComplianceProject ManagementBusiness DevelopmentClinical TrialsClinical ResearchResearchLeadershipCollaborationMentoringBiostatistics

About the role

  • 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.
  • About Allucent Our mission is to help bring new therapies to light.
  • Si ce poste vous intéresse, veuillez postuler en cliquant sur le bouton ci-dessous.

Responsibilities

  • 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.
  • 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.
  • In addition to managing project timelines, budgets, and deliverables, you'll drive process improvements, contribute to business development activities, and provide technical leadership and mentorship to junior team members.
  • We're looking for a Senior Clinical Programmer I who thrives on solving complex challenges and transforming clinical data into high-quality, reliable insights that drive drug development.
  • You'll collaborate cross-functionally to design, build, validate, and maintain clinical databases, develop programming solutions and data visualizations, and champion CDISC standards and programming best practices.

Requirements

  • If you are interested in this role please apply through the button or for more information reach out to Demetria Eggleston at Demetria.eggleston@allucent.c

Nice to have

  • Découvrez-en plus sur nos valeurs.

Company info

  • Find more information about our values.
  • At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

This listing is sourced directly from Allucent's careers page and normalized into a canonical job model.