Experience

PsycIME

• Canada
• Medical Practices
• 1 - 100 Employee

• Senior Psychiatrist Administrative Lead

  • Jan 2022 - Present



Ontario Institute for Studies in Education of the University of Toronto

• Canada
• Higher Education
• 300 - 400 Employee

• Research Practicum

  • Sep 2021 - Present



Lyptus Medical

• Mexico
• Hospitals and Health Care
• 1 - 100 Employee

• Mental Health Specialist

  • Jan 2019 - Present



Hospital Ángeles Lomas

• Mexico
• Medical Practices
• 1 - 100 Employee

• Psychiatrist

  • Sep 2011 - Dec 2021



Mexican Sleep Academy

• Secretary

  • Jan 2014 - Jan 2016



HOSPITAL ISSEMYM

• Hospitals and Health Care
• 1 - 100 Employee

• Clinical Research Assistant

  • Feb 2006 - Jan 2007

  • Interact with personnel from study sponsors, investigational sites, vendors to enable timely and high quality initiations and completions of clinical trials. • Compile documentation for qualification of clinical sites. Support review of that documentation to ensure that those clinical sites comply with ICH-GCP and relevant local regulations. • Assist with preparation and submission of regulatory documents to responsible authorities and IRB/ECs. • Responsible for set-up and maintenance of studies in Clinical Trial Management System (CTMS) and Trial Master File (TMF). • Contribute to the development of documents that facilitate or describe the management of the clinical trial. Examples of such documents include, study guides or manuals, and information collection tools. • Assist in review of documentation of information provided to study subjects, including informed consent forms. • Assist in working with meeting planners and vendors to arrange for investigator meetings, off-site client or internal departmental meetings. • Responsible for the shipment and tracking of trial documents (site binders, manuals, guides, etc.) • Record and inventory visit reports received from monitoring staff. • Maintain study portals, web sites, or newsletters. • Compile reports progress/status of investigational sites. • Assist with processing vendor invoices, investigator payments, and expense reports. • Participate in the development and maintenance of, and adhere to departmental Standard Operating Procedures (SOPs) and guidelines. • Maintained and prepared for final archival of documents relevant to the assigned clinical trials, and assisted the corporate archivist in assembling and archiving such documents. • Assisted data management quality assurance (QA) personnel in performing QA procedures on trial Case Report Forms (CRFs), database schema and databases for assigned studies. Show less