Rebekah Tassone

WORK HISTORY

EDUCATION

ABOUT REBEKAH TASSONE

I am an accomplished program management leader with 10+ years of experience directing global pharmaceutical development programs from pre-IND through commercialization across varying therapeutic areas. Expertise in strategic risk management, milestone planning, and cross-functional collaboration to accelerate clinical development, align regulatory and manufacturing timelines. Proven success in process optimization, executive reporting, capability building, and risk mitigation. Skilled in vendor management, regulatory compliance (ICH/GCP), and team leadership, driving operational excellence across clinical, analytical, and quality initiatives.I thrive on fostering collaboration across cross-functional teams, managing vendor relationships, and navigating complex regulatory timelines. My experience includes directing specialized teams focused on analytical and quality initiatives, supporting department-wide budget planning, and facilitating communication across Clinical, Product Manufacturing, Quality, and Regulatory teams.Passionate about maintaining high-quality standards, I have a proven track record of auditing quality systems and coordinating critical regulatory submissions throughout all clinical study phases. I am committed to driving innovation and excellence in every project I undertake, and I look forward to contributing my expertise to future endeavors.