Provide strategic statistical leadership across oncology development programs, collaborating with Clinical Development, Regulatory, Medical, Commercial, and Portfolio teams.
Design and validate trial types, endpoints, and innovative adaptive designs while performing sample size/power calculations and establishing go/no-go decision gates.
Support regulatory submissions and health authority interactions, and quantify technical success probability for pipeline prioritization.
We are a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, we are committed to training, diversity, and accelerating innovative drug and device development.
Lead the clinical development of respiratory disease programs, overseeing study design, execution, and delivery across the development lifecycle.
Provide scientific oversight to ensure patient safety, study quality, and timely delivery while generating and interpreting clinical evidence.
Collaborate with cross-functional teams and external stakeholders to align clinical strategies with regulatory, commercial, and patient needs.
They are a pharmaceutical company focused on advancing clinical research and developing innovative treatments for respiratory diseases. The organization fosters an inclusive, collaborative culture that prioritizes patient impact, professional growth, and scientific innovation.
Drive and execute clinical research and real-world evidence across the product portfolio.
Design protocols, statistical analysis plans, and support regulatory activities.
Generate evidence for product development, reimbursement, and scientific dissemination.
Sequel develops next-generation drug-delivery technology, starting with the twiist Automated Insulin Delivery (AID) System for diabetes management. The company fosters a culture of hard work, fun, and genuine support, with a strong focus on employee well-being and comprehensive benefits.
Serve as study statistician for Phase 1-3 vaccine clinical trials, leading statistical design, analysis, and reporting.
Oversee statistical CROs, develop analysis plans, and ensure regulatory and scientific rigor.
Provide statistical consultation across CVIA programs and represent PATH at scientific meetings.
PATH is a global nonprofit dedicated to achieving health equity, developing and scaling innovative solutions to pressing health challenges. With more than 40 years of experience, PATH fosters a culture of collaboration and partnership across diverse teams.