Daniel Cher, Md
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Daniel Cher, Md Email & Phone Number

Expert in US and EU regulatory affairs, clinical trial design, execution, analysis, and reporting for medical device manufacturers. at SI-BONE
Location: Palo Alto, California, United States 11 work roles 2 schools
1 work email found @wildirisconsulting.com 3 phones found area 650 LinkedIn matched
✓ Verified August 2026 4 data sources Profile completeness 100%

Contact Signals · 1 work email · 3 phones

Work email d****@wildirisconsulting.com
Direct phone (650) ***-****
LinkedIn Profile matched
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Current company
Role
Expert in US and EU regulatory affairs, clinical trial design, execution, analysis, and reporting for medical device manufacturers.
Location
Palo Alto, California, United States

Who is Daniel Cher, Md? Overview

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Quick answer

Daniel Cher, Md is listed as Expert in US and EU regulatory affairs, clinical trial design, execution, analysis, and reporting for medical device manufacturers. at SI-BONE, based in Palo Alto, California, United States. AeroLeads shows a work email signal at wildirisconsulting.com, phone signal with area code 650, and a matched LinkedIn profile for Daniel Cher, Md.

Daniel Cher, Md previously worked as Sr. Vice President of Clinical and Regulatory Affairs at Si-Bone and Vice President of Clinical Affairs at Si-Bone. Daniel Cher, Md holds Doctor Of Medicine (M.D.), 1990 from Yale School Of Medicine.

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Email format at SI-BONE

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*@wildirisconsulting.com
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Profile bio

About Daniel Cher, Md

General internist with >25 years' experience in medical devices. I help companies develop efficient and effective clinical and regulatory strategies for new medical devices. Excellent track record in class II and III devices. Expertise in statistics. Primary statistician on 4 PMAs, 1 de novo and several 510ks. Participated in 4 breakthrough designations.Email: djcher@gmail.com

Listed skills include Medical Devices, Fda, Regulatory Affairs, Clinical Trials, and 24 others.

Current workplace

Daniel Cher, Md's current company

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SI-BONE
Si-Bone
Expert in US and EU regulatory affairs, clinical trial design, execution, analysis, and reporting for medical device manufacturers.
AeroLeads page
11 roles · 29 years

Daniel Cher, Md work experience

A career timeline built from the work history available for this profile.

Sr. Vice President Of Clinical And Regulatory Affairs

Current

Santa Clara, California, Us

Leading regulatory and clinical strategies at a public medical device company focused on sacroiliac joint fusion and pelvic fixation devices. Several positive 510ks, 2 breakthrough device designations and EU MDR certification.

Jun 2021 - Present

Vice President Of Clinical Affairs

Santa Clara, California, Us

Develop and lead team to execute clinical trials at medical device manufacturer (SI-BONE). iFuse Implant System is indicated for the treatment of sacroiliac joint dysfunction. I designed, oversaw execution, analyzed and reported 5 prospective clinical trials, including two landmark surgery vs. non-surgery randomized trials. Now over 70 publications with clinical outcomes data. Strong clinical data allowed company to achieve financial goals (IPO) in 2018.

Jan 2012 - Jun 2021

President

Current
Wild Iris Consulting Llc

Have helped >15 medical device companies in clinical trial design, statistical analysis, report writing, FDA negotiations, power analysis, web-based data collection tools. Converted several rejected IDEs into approved IDEs. Rapidly help CEO to develop clinical and regulatory strategies.

Jan 2004 - Present

Vice President Of Medical Affairs, Head Of Biostatistics

San Jose, California, Us

Oversee medical affairs and biostatistics for growing medical device company with waterjet-based resection technology for benign prostatic hyperplasia.

Jan 2018 - Mar 2021

Vice President Of Regulatory And Quality Affairs

San Jose, California, Us

Head of regulatory and quality affairs for start-up medical device company with semi-automated image-based robot used in the treatment of benign prostatic hyperplasia. Helped company to obtain market approval in the US through work with US FDA.

Jan 2017 - Jan 2018

Vice President Of Clinical/Regulatory Affairs

Hourglass Technologies Inc.

Obtained approvals for FIM clinical trials of novel obesity device. Company closed for lack of funding.

Jul 2011 - Jul 2012

Vice President Of Clinical And Regulatory Affairs

Chestnut Medical Technologies

Obtained PMA appproval in 3 years for ground-breaking neurovascular device with single-arm clinical trial. Led clinical and regulatory teams. Company acquired by ev3 in 2009 and Covidien in 2010.

May 2008 - Mar 2012

Vice President Of Clinical And Regulatory Affairs

Pulmonx

Head of clinical and regulatory affairs at medical device start-up focusing on products for patients with emphysema

Mar 2007 - Jan 2008

Vice President Of Clinical Research

Us

Head of clinical research at a large orthopedic product medical device company

Sep 2006 - Mar 2007

Medical Director

Us

Head of clinical and regulatory affairs at a small medical device start-up focusing on products for cardiac ablation

Oct 2003 - Sep 2004

Statistician

Primary statistical analysis for FDA submission of a novel class III product. Used Bayesian statistics to allow submission 3 months early.

1998 - 2000 ~2 yrs
2 education records

Daniel Cher, Md education

Doctor Of Medicine (M.D.), 1990

Yale School Of Medicine

Bs, Biology

Stanford University
FAQ

Frequently asked questions about Daniel Cher, Md

Quick answers generated from the profile data available on this page.

What company does Daniel Cher, Md work for?

Daniel Cher, Md works for SI-BONE.

What is Daniel Cher, Md's role at SI-BONE?

Daniel Cher, Md is listed as Expert in US and EU regulatory affairs, clinical trial design, execution, analysis, and reporting for medical device manufacturers. at SI-BONE.

What is Daniel Cher, Md's email address?

AeroLeads has found 1 work email signal at @wildirisconsulting.com for Daniel Cher, Md at SI-BONE.

What is Daniel Cher, Md's phone number?

AeroLeads has found 3 phone signal(s) with area code 650 for Daniel Cher, Md at SI-BONE.

Where is Daniel Cher, Md based?

Daniel Cher, Md is based in Palo Alto, California, United States while working with SI-BONE.

What companies has Daniel Cher, Md worked for?

Daniel Cher, Md has worked for Si-Bone, Wild Iris Consulting Llc, Procept Biorobotics, Hourglass Technologies Inc., and Chestnut Medical Technologies.

How can I contact Daniel Cher, Md?

You can use AeroLeads to view verified contact signals for Daniel Cher, Md at SI-BONE, including work email, phone, and LinkedIn data when available.

What schools did Daniel Cher, Md attend?

Daniel Cher, Md holds Doctor Of Medicine (M.D.), 1990 from Yale School Of Medicine.

What skills is Daniel Cher, Md known for?

Daniel Cher, Md is listed with skills including Medical Devices, Fda, Regulatory Affairs, Clinical Trials, Clinical Research, Start Ups, Orthopedic, and Iso 13485.

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