Teresa Accettura
About Teresa Accettura
Teresa Accettura is a Global Trial Specialist at Bristol Myers Squibb and a Post Graduate Year 2 Pharmacy Resident at Oncology Institute Professor Doctor Alexandru Trestioreanu in Bucharest, Romania.
Current Positions
Teresa Accettura is currently a Global Trial Specialist at Bristol Myers Squibb. She additionally serves as a Post Graduate Year 2 Pharmacy Resident at the Oncology Institute Professor Doctor Alexandru Trestioreanu in Bucharest, Romania. These roles involve significant responsibilities in clinical trials and pharmacy practice.
Professional Background
Teresa has accumulated diverse professional experiences. She worked at PSI CRO AG as a Clinical Trial Administrator I from 2019 to 2020 in Bucharest, Romania. Before that, she served as a Documentation Officer in QA/QC at Labormed Alvogen from 2018 to 2019. These roles have provided her with a strong foundation in clinical trial administration and quality assurance/control.
Role at Bristol Myers Squibb
Teresa began her tenure as a Global Trial Specialist at Bristol Myers Squibb on January 1, 2021. In this role, she contributes to the planning, execution, and management of global clinical trials. This position leverages her expertise in clinical trial administration gained from previous roles, providing a critical function in the company's research and development pipeline.
Educational Background
Teresa Accettura holds a Doctor of Pharmacy (PharmD) degree from the University of Medicine and Pharmacy "Carol Davila," achieved after five years of study from 2014 to 2019. She furthered her education with a Post-Graduate Degree in Clinical Pharmacy from the same institution, completed between 2020 and 2023. This advanced education underscores her comprehensive expertise in both general and clinical pharmacy.
Clinical Trial and QA/QC Experience
Teresa's experience spans roles in clinical trial administration and quality assurance/quality control. At PSI CRO AG, she gained hands-on experience in clinical trial management as a Clinical Trial Administrator I. Her role as a Documentation Officer in QA/QC at Labormed Alvogen involved focusing on quality assurance and control documentation. These positions have equipped her with essential skills and knowledge for her current roles.