Amy Feehan Curley

About Amy Feehan Curley

Motivated and industrious research professional with extensive experience in academia, healthcare, and pharmaceuticals. Success built from engaging across multitude of specialties and projects. Quick to master new therapeutic areas as evidenced by PhD training in neuroscience, publications in top infectious disease journals, and successful NDA submissions in oncology (Hernexeos). Independent worker and effective collaborator, always using creativity, innovation, and relentless nature to problem solve challenges and move projects forward. Passion for strategic, patient-centric clinical trial designs, improving equity and inclusion in clinical trials, and STEM outreach for K-12 and science communications. Recognized for being energetic and enthusiastic, always promoting harmony among teams, positive communication, constructive feedback, and hard work to achieve results.

Experience

1. Feasibility & Planning Manager, Oncology

   Boehringer Ingelheim

   Feb 2026 — Present · US

   Leads comprehensive, data-driven feasibility assessments for global clinical studies, integrating epidemiologic data, historical performance, real-world evidence, and site intelligence to guide country and site selection, improve enrollment predictability, and inform strategic recommendations.• Translates complex protocol requirements into clear operational criteria, ensuring study designs are executable, realistic, and tailored to patient and site capabilities; collaborates with Country and Regional Feasibility Managers to validate assumptions and incorporate local market dynamics and site feedback.• Serves as the strategic feasibility liaison for cross-functional stakeholders, presenting findings and risk assessments to governance bodies and senior leaders to influence decisions on study design, site strategy, and operational approach.• Drives continuous improvement by leveraging advanced analytics, automation, and emerging technologies to enhance feasibility workflows, ensure regulatory and ethical compliance, and support efficient, high-quality clinical trial execution.• Communicates complex findings clearly and concisely to cross-functional teams and senior decision-makers, enabling data-informed planning and governance approvals in a complex global environment.

Education

• Tulane University

  Bachelor of Science (BS), Neuroscience

  2008 — 2011

• Tulane University

  Doctor of Philosophy (PhD), Neuroscience

  2014