Hector A. Email & Phone Number

An experienced leader in Immunology with a focus on project management, process improvement, and analytical method development. Over several years experience in the biopharmaceutical industry.* Excellent knowledge in pharmaceutical/Clinical/preclinical research in GCP and GLP* GCP, GLP trained* Expertise in scientific project managing * Excellent staff supervision and management skills* Excellent problem resolution skills* Excellent competences in quality control of documents* Very good computer skills and knowledge of Word, Excel and Adobe Acrobat* Strong team spirit* Great autonomy, adaptation and learning qualities *Trilingual: English, French and Spanish

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  Senior Scientist

  Altasciences

  Nov 2022 - Present - Laval, Quebec, Canadá

  Act as Study Director/Principal Investigator of R&D and validation of analytical methods (LBA, ELISA, QPCR, RT-QPCR and others).• Ensure the coordination of several projects simultaneously (personnel, materials, instruments, deadlines, customer requirements and others)• Supervise/Mentor scientists and technical staff.• Manage bioanalytical activities in support of toxicology, biodistribution and bioequivalence studies.• Write/review various study documents in compliance with FDA and OECD requirements (Standing Operating Procedures, Study Protocols, Study Reports, Deviations, Investigations, CAPAs, Ethics Committee (IRB) Forms and consent forms (ICF), import/export forms and others).• Verify the quality and integrity of study documents and the consistency of results.• Analyze and interpret results (pharmacokinetics (PK), Anti-drug antibodies (ADA), biomarkers (BA), and others).• Manage inventory and use of study samples• Monitoring of study budgets.• Prepare Statements of Work (SOW)