Journal of Bioequivalence & Bioavailability

Teresa Nunes

Biography

Teresa Nunes is experienced pharmaceutical physician with more than 12 years in the industry covering operational, medical and safety management of Phase I to Phase III studies. Teresa Nunes is also familiar with small molecules, proteins, antibodies and other biologicals, Global drug development/approval experience in CNS, Cardiology, Oncology and Orphan Diseases. Experience in adult and pediatric drug development. She has successfully lead Line management experience of cross functional teams and responsible for the clinical and operational strategy during drug development, having actively contributed to the design and implemention of several drug development plans, leading the development up to market stage. Participated in meetings with regulatory agencies (e.g. pre IND/end of phase 2/pre NDA meetings) not only in EU but also US and participated in site and vendor audits as the clinical team member. Contributed to the successful out licensing of drug candidates in the development stage. During her career she was also actively involved in risk and safety management of marketed drugs.Published over 40 peer reviewed articles and more than 75 scientific abstracts presented at meetings.

Research Interest

Oncology Neurology Pharmacovigilance