As Clinical Program Director, you will develop and maintain global clinical evidence plans aligned with therapy objectives, product development milestones, and regulatory requirements. You will lead the execution of industry-sponsored clinical trials in collaboration with CROs, specialized vendors, and consultants, overseeing study design, patient recruitment, and data quality. You will ensure studies are delivered on time, within budget, and in compliance with GCP, ISO 14155, and applicable regulations.
You will work closely with Leadership, Market Access, Regulatory, R&D teams to ensure study design supports product development and approval strategies. You will collaborate with clinical scientists and biostatisticians on endpoint selection, statistical analysis plans, and data interpretation.
You will identify, engage, and develop relationships with global and regional KOLs to guide clinical strategy and enhance program credibility, fostering long-term KOL relationships to support ongoing evidence generation, scientific exchange, and therapy adoption.