General Surgery Research Team

Our team supports Faculty research in the 6 sections of General Surgery; Acute Care Surgery, Surgical Oncology, Colorectal Surgery, Endocrine Surgery, Minimally Invasive/Bariatric Surgery and Hepatobiliary Surgery.

Stanford School of Medicine Clinical Research Units (CRUs) were created to provide oversight and support for all clinical trials and clinical research protocols in the CRU portfolio. We provide protocol development, regulatory and study management and financial review in partnership with the Stanford IRB and School of Medicine’s Research Management Group.

Our Biostatistics Core supports clinical research from concept to completion. In the early phases, we provide guidance on study design, run sample size calculations, and develop statistical analysis plans. Our services continue through data analysis, and we collaborate with teams to interpret and present results, including preparation and submission of abstracts and manuscripts.

The development of this unit continues to further our mission to drive innovation in clinical research within General Surgery. By providing comprehensive research support and fostering collaboration, we aim to enhance the quality and impact of research within the Division, ultimately improving patient outcomes and advancing the field of surgery.

Our team is available to collaborate on clinical trials, research and biostatistical projects in the Division of General Surgery.

Consult With Us

Research Services Offered

  • Management of the entire life cycle of clinical trials & studies
  • IRB submissions
  • Data Use Agreements
  • Budget Preparation
  • Patient consenting and enrollment
  • Data collection

 

Biostats Services Offered

  • Study design
  • Statistical analysis plans
  • Sample size calculation
  • REDCap database creation
  • Qualtrics survey creation
  • Analysis consultation
  • Interpretation of results
  • Statistical analyses
  • Preparation for publication

For questions or to initiate a project with our team, please complete the Research Intake Form:

Timeline

Research Services

Keep the following in mind and plan accordingly:

  • 4+ months for a DUA
  • 90+ days for a budget with RMG
  • 4-5 months for clinical trial initiation at Stanford
  • 4-6 weeks for IRB review for regular protocols (expedited protocols reviewed sooner)

Biostats

The following are preferred for biostats services:

  • 4-6 months for study design
  • 4 weeks for conference abstracts
  • 3 months for manuscripts

Our Team

Anisha Abreo

Clinical Research Manager

(650) 498-2796
aabreo@stanford.edu

 

Renceh Flojo

Associate Clinical Research Coordinator

(650) 724-2877   rflojo@stanford.edu

Alexandra Antoinette Myers

Senior Clinical Research Coordinator

(650) 498-3284
amyers19@stanford.edu

 

 

Michelle Earley

Biostatistician II

(650) 724-8445
mjearley@stanford.edu

Jonathan King

Biostatistician I

(650) 498-8632
jmking@stanford.edu

Jacqueline Chang

Associate Clinical Research Coordinator

(650) 497-7973   cjackie@stanford.edu

Leora Cohen-Tigör 

Associate Clinical Research Coordinator

(650) 497-8332  lcohenti@stanford.edu

Jadis Chen

Associate Clinical Research Coordinator

(650) 497-9737  jadis@stanford.edu