Directory of Consultants
Bay Area Biomedical Consultants Network (BABCN)
Name and Educational Degree(s) de Boer, Corine, MD, PhD
Business Name Tulip Medical Consulting LLC

Please see my LinkedIn profile: http://www.linkedin.com/in/corinedeboermdphd

Business Address Office locations in SF Bay Area and greater Seattle area
For mailing address please contact us by e-mail, CA 94710 WA 98368
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Vaccines (cancer and ID), Adjuvants, Biologics, Infectious Disease incl Meningococcal Disease, HIV/AIDS and Hepatitis B, Immunology, Nephrology, Metabolic Disorders (incl PKU) and Pediatrics (Oncology, Metabolic Diseases, Cystic Fibrosis, Gastroenterology)


Tulip Medical Consulting, LLC. is a physician consulting service organization started in October 2010 by Corine de Boer, MD, PhD to provide strategic, logistical and operational clinical research development services to biotechnology and pharmaceutical companies.

Dr. de Boer has 20 years experience designing, conducting and analysing a variety of international pre-clinical and phase-1 through phase-4 clinical trials. She has provided support for a variety of vaccines, adjuvants and biologics from discovery to launch including commercial support and scientific publications. Prior to launching Tulip Medical Consulting, LLC., Dr. de Boer worked for nearly a decade in the bio-pharmaceutical industry initially at Chiron Corporation and Novartis Vaccines & Diagnostics and most recently as Senior Director, Clinical Development at Dynavax Technologies where she was responsible for their phase-3 Hepatitis B vaccine program in chronic kidney disease patients.

Tulip Medical Consulting, LLC. can provide you with the following services specifically tailored to meet your company's needs:

  • Clinical expertise in Pediatrics, Vaccinology, Immunology, Infectious Disease and Nephrology
  • Scientific advice on identification of appropriate clinical endpoints, surrogate markers and patient population for your product
  • Preparation and Review of IND and CTA submissions (non-clinical and clinical sections)
  • Strategic input in Clinical Development decision-making
  • Design of and advice on Clinical Development Plans
  • Writing and review of clinical protocols, Investigator Brochures, Clinical Study Reports and other study-related documents
  • Participation in and preparation of ad-hoc and scheduled meetings with FDA and other global regulatory authorities
  • Selection, management and oversight of investigational clinical sites, Contract Research Organizations and other vendors
  • Leadership of clinical trials including Medical Monitoring and line-management oversight
  • Organization and participation in Data Monitoring Committee (DMC) and SEAC (Safety Evaulation and Adjudication) activities
  • Interpretation & analysis of clinical trial results
  • Preparation and review of BLA sumbissions
  • Development and successful maintenance of critical relationships with key opinion leaders, advocacy groups and scientific organizations
  • Competitive analysis
  • Commercial support throughout the product life cycle

CV and References available upon request

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