Ana Gomes

Ana Gomes is a highly experienced Senior Regulatory Writer at Bioscript Group since September 2022, with a robust background in medical writing and regulatory affairs. Prior to this role, Ana served as a Medical Writing Coordinator and Medical Writer at BlueClinical, where responsibilities included overseeing clinical study documentation and managing Medical Writers to ensure compliance. Previous positions also include Associate Regulatory Affairs Manager and Clinical Trials Assistant at Blueclinical, as well as roles in pharmaceutical regulatory consultancy and academia. Ana's academic credentials include a PhD in Pharmaceutical Chemistry, a Master of Science in Quality Control, and a Licenciate degree in Pharmaceutical Sciences from Universidade do Porto and Instituto Superior de Ciências da Saúde-Norte.