Theresa R. Devins, PhD

Multidisciplinary expertise with 20+ years clinical research experience as International Lead, landmark studies. Extensive expertise in international and national clinical study leadership and international/national regulatory requirements. Advanced degrees in Public Health and Clinical Research Administration. Key author of two white papers on increasing minority patients in clinical trials and retention strategies in longterm outcome trials. Specialist in diversity in clinical trials including change mechanisms to ensure sustainability. Strong science background with special interests in precision medicine and pharmacogenomics. External collaboration and partnerships with FDA, PhRMA and TransCelerate Biopharma. Demonstrated expertise in international matrix management, including cultural sensitivity and direct line management. Excellent communication skills and strategic planner. Highly adaptable, well-organized, self-motivated and ongoing process assessment to increase efficiencies, reduce costs and expedite timelines. Works well in a team setting as well as management positions. Therapeutic experience includes cardiovascular, respiratory, metabolic, infectious diseases, pediatric and adult oncology.