Jose Trigo, Phd Email & Phone Number

Baltimore, MD, US

• Responsible for providing Scientific Input and Clinical Operations expertise and in the Development of the Clinical Trial protocol, and other study documents, overall strategy and objectives of clinical plans and.
• Support the execution of clinical development and operations (Phase II-IV) strategies and implementation of new processes and systems. Contribute to cross-functional initiatives as Subject Matter Expert (SME).
• Review and approve study documents as needed, e.g., Communications Plans, Study Plans, Study Initiation Visit, Training, Trial Master File Plan, etc.
• Participate in Inspection Readiness efforts and in preparation for regulatory submissions.

Baltimore, Maryland Area

• Battelle is the largest independent nonprofit applied science and technology organization in the world. Battelle's Public Health comprehensive solutions include cross-disciplinary scientific and engineering.
• Leadership and management of large multidisciplinary research programs (over $10M) and clinical development teams, contracts, key opinion leader relationships.
• Oversight of the overall execution of the assigned clinical trial programs (study start-up, enrollment, study conduct, close out, etc.).
• Led the strategy and tactics to successfully work with key stakeholders, company leaders, vendors, investigators, and cross-functional departments to develop, implement and deliver clinical studies/programs.
• Ensured clinical study project plans, timelines, and budgets were aligned with the goals of the overall development program needs.
• Make decisions and recommend operational strategies in support of achieving clinical program objectives.

Région De Toronto, Canada

• The Centre for Addiction and Mental Health (CAMH) is Canada's largest mental health teaching hospital and one of the world's leading research centres.Responsibilities:
• Led large and complex deliverables and managed clinical trials (Phase II-IV) in CNS (total over $15M).
• Led strategies for patient recruitment and retention in clinical trials.
• CROs evaluation, selection and oversight. Point of escalation for CROs partners as appropriate.
• Oversight and accountability for program budgets, staffing, and timelines.
• Maintained awareness of industry trends/developments for the future strategic direction of clinical programs.

• The Universitat Pompeu Fabra (UPF) was founded in 1990 and is a modern, prestigious public university, which is consistently ranked among the top European universities.Responsibilities:
• Established pre-clinical models of psychiatry and clinical pharmacology, including medical devices, to allow testing of novel CNS drug candidates on a behavioral, physiological, and molecular level.
• Supervised research projects, including developing and executing research projects, data analysis, and communicating findings to the scientific community (total over $8M).
• Delivered scientific presentations to peers in seminars and lab meetings.
• Mentored, supported and trained research staff.

Phd, Neurosciences

Master'S Degree, Neurobiology And Neurosciences

Bachelor'S Degree, Psychology