Brandon Doyle

About Brandon Doyle

20 years of clinical research trial experience across a broad range of therapeutic areas; oncology, cardiology, and pulmonology• Global site solution subject matter on diversity, equity and inclusion. Membership of SCRS Diversity Working Group and Membership CISCRP Diversity Committee.• Experience in multiple roles within clinical research: Research Assistant, Clinical Research Coordinator, Patient Recruitment, Project Management, and Site Management • Effective communication skills with extensive experience presenting business analysis and strategic operational recommendations • Significant experience working with the FDA and IRB/IEC regulations and regulatory compliance while meeting GCP/ICH guidelines• Team oriented work ethic; ability to work with diverse persons and work styles• Strong organizational skills and time management abilities, as evidenced by rapid progression into greater leadership roles. An innovative troubleshooter who quickly identifies a problem and investigates more efficient best practices• MBA with an emphasis in Management: Courses included Managing People and Organizations, Operations Management, Negotiations, and Research Statistics• Fluent in Spanish

Experience

1. Associate Director, Study Site Engagement

   Takeda

   Oct 2023 — Present

Education

• UMN Carlson School of Management

  MBA, Marketing and Management

  2005 — 2008

• University of Minnesota

  Bachelor of Arts, Sociology and Psychology

  1996 — 2002

Skills

• Oncology
• Protocol
• Management
• Edc
• Ctms
• Clinical Research
• Market Research
• Excel
• Gcp
• Powerpoint
• Microsoft Excel
• Leadership
• Research
• Protocol Development
• Irb
• Spss
• CRO
• Study Design
• Good Clinical Practice (Gcp)
• Clinical Trials
• Clinical Development
• Electronic Data Capture (Edc)
• Protocol Writing
• Patient Recruitment
• Microsoft Office
• Qualitative Research
• Healthcare
• Pharmaceutical Industry
• Sop
• Data Analysis
• Clinical Study Design
• Fda