Invests in
Locations:
Min Investment:
$100,000.00Max Investment:
$5,000,000.00Target Investment:
$1,500,000.00
Skills
Education
- U-
- U-
Lists including Marcelo
Work Experience
2023
Independent Board Member and Chairman of the Science and Technology Committee
2023
2023
Board Member
2023
Santa Ana Bio leverages deep cell profiling technologies, to design precision biologics in the innate immunity space.
2019
President and CEO
2019
2019 - 2023
Venture Partner
2019 - 2023
2019 - 2022
Board Member - Coda Biotherapeutics
2019 - 2022
2018 - 2019
Chief Medical Officer, SVP
2018 - 2019
Responsible for general medical governance and patient safety oversight relating to all Purdue products, as well as of its subsidiaries, in development and in the market.
2014 - 2018
Head of Specialty Research and Development & Chief Scientific Officer
2017 - 2018
Leading all specialty research and development, including discovery, early and late stage clinical development, safety and pharmacovigilance, as well setting scientific priorities for the specialty pipeline.
Chief Medical Officer & Head of Global Specialty Clinical Development
2017 - 2017
Head of a group with over 600 employees, in charge of Global Early Stage Clinical Development, Global Late Stage Clinical Development, Global Safety and Pharmacovigilance and Global and Regional Clinical Operations, Biometrics and Data Management. Reports to the President of Global R&D.
Head of Global Specialty Development - Teva Pharmaceuticals
2016 - 2017
Responsible for directing and leading the Clinical Development (Phases 1 to 3),across all specialty areas at Teva. Areas include Migraine/Headaches, Pain, Neurodegeneration, Movement Disorders, Multiple Sclerosis, Respiratory, and others. Responsible for leading the Clinical Pharmacology, Global Clinical Operations and Biometrics groups as well. Reports to the President, Global R&D.
Senior Vice President, Head of Clinical Operations & Innovations and TA Head, Migraine & Headaches
2015 - 2016
Head of R&D group housing Global Clinical Operations, Clinical Pharmacology, Global Biometrics and Global Medical Writing. Therapeutic Area head for the Migraine and Headache programs.
Vice President, Migraine & Headache, Clinical Development R&D at Teva Pharmaceuticals
2014 - 2015
Responsible for all R&D activities required to support the development of medications in migraine and pain, including the development of LBR-101, a monoclonal antibody against CGRP, and of Zecuity, the novel iontophoretic patch for the acute treatment of migraine. Also responsible for providing key strategic input to any further business development activities the company in this field.
2013 - 2014
Chief Medical Officer
2013 - 2014
Responsible for heading the research development of a humanized monoclonal antibody targeting CGRP, a molecule of relevance in migraine and pain. Direct reports include Head of Preclinical Research, VP of Clinical Operations and VP of Regulatory Affairs.
2007 - 2013
Head of the Merck Investigator Study Program, Scientific Engagements and Education
2010 - 2013
* Head of an organization that encompassed 13 research committees and is responsible for the review of over 1300 research proposals per year, and for the funding of over 400 studies per year across all therapeutic areas of interest to Merck. The division also reviews company initiated non-regulatory studies globally. Department consists of nearly 40 employees/contractors * Head of scientific education, or the development of unbranded curriculum on drug development for use at academic institutions. * Manager of 5 M.D. Global Executive Directors covering scientific affairs in the areas of HIV, Hepatitis, Anti-Infectious diseases, Ophthalmology, Anesthesiology, and Oncology.
Global Director for Scientific Affairs, Neurology and Psychiatry
2007 - 2010
Responsible for scientific and medical affairs in neurology and psychiatry. Developed the scientific leadership strategy for both areas at Merck (including chairing investigator initiated study programs, running advisory boards)
2006 - 2007
Director of Research
2006 - 2007
Responsible for the execution of clinical trials (phase 1 to 3), as well as for the development and funding of investigator initiated studies. Over 30 studies conducted during tenure.