This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
You will lead the RTSM (Randomization and Trial Supply Management) function in the United States. You will partner with clinical development, operations, quality and external vendors to design and deliver patient-focused randomization and clinical supply solutions. We value clear decision-making, pragmatic problem solving, and inclusive leadership. You will shape strategy, build capability, and drive consistent delivery for clinical studies. This role offers strong growth, real impact on patients, and the chance to work where science, technology and talent come together to get ahead of disease.
Job Responsibility:
Lead design and delivery of RTSM strategies across Phase I–IV clinical programs and investigator-sponsored studies
Direct cross-functional teams and vendors to ensure on-time randomization, kit assignment, and clinical supply availability to sites and patients
Own risk assessments and contingency plans for trial supply and randomization activities
Establish and improve RTSM processes, metrics, and governance to drive quality and efficiency
Partner with clinical operations, biostatistics, data management, and regulatory functions to align RTSM with study design and compliance needs
Hire, coach and develop a diverse team, and foster collaboration across internal and external partners
Requirements:
Bachelor's degree in life sciences, pharmacy, engineering, IT, or related field, or equivalent experience
8+ years of experience managing RTSM, IRT, or clinical supply systems in the pharmaceutical or biotech industry
Experience leading cross-functional teams and managing external vendor relationships
Experience with clinical trial operations, randomization methods, blinding and investigational product supply principles
Experience with system vendor selection, implementation, validation, and change control
Nice to have:
Advanced degree in a relevant discipline or equivalent senior leadership experience
Experience with eClinical ecosystems, integrations between RTSM and clinical systems, and data flows
Background in global trial support and managing multi-region supply and regulatory requirements
Proven track record of building and mentoring high-performing teams
Experience implementing process improvements, metrics and dashboards to measure RTSM performance
Knowledge of relevant regulations and GxP expectations for clinical supply and systems
Clear communication skills with experience presenting to senior stakeholders and managing escalations