Strategic Development and Representation for
Biotech, Device and Pharmaceutical Companies

(720) 746-1190 Tel
(720) 746-1192 Fax
info@cbrintl.com

Current Job Openings at CBR International:

Manager of Clinical Writing and Operations

Clinical Affairs Associate

Manager of Quality Assurance

Manager of Non-Clinical Strategy

Head of Technical Writing

Regulatory Specialist: Devices/Combination Products

Scientist/Consultant

Scientist/Writer

Medical Officer

Project Associate

eSubmissions Associate

Administrative/Operations Associate


General Career Opportunities at CBR:

Scientists/Consultants – Master's or Ph.D. (biochemists, biologists, pharmacists, neuroscientists, etc.); focused on advising clients in biotech, pharmaceutical, and medical device development, through FDA.

Scientists/Technical Writers – Master's or Ph.D. (biochemists, biologists, pharmacists, neuroscientists, etc.); focused on technical research and regulatory development.

Clinical Writers – Advanced degree; focused on developing clinical protocols and study documents.

Clinical Operations – Bachelor's or above; focused on overseeing clinical trials and trial documentation.

Regulatory Scientists – Bachelor's or above; focused on Regulatory Affairs processes in US and EU.

Quality Scientists – Bachelor's or above; focused on review of product formulation, testing, and stability.

Project Associates – Associate's or Bachelor's; focused on support for and participation in technical programs.

eSubmissions – Associate's or Bachelor's; focused on electronic publishing for regulatory submissions.

Administrative/Operations – Associate's or Bachelor's; focused on office administration and business operations.


We are Expanding and We're Hiring!
CBR is growing! We have numerous opportunities for professionals at all levels. Some of these positions are available in the D.C. metro area, Atlanta, San Francisco, and San Diego.

If you are interested in applying for a position at CBR, please send a cover letter and resume to HR@cbrintl.com.

What We Do

We provide expert services in the following areas:

  • US & EU Regulatory Representation
  • Biotech Product Development
  • Process & Methods Validation
  • Nonclinical Development Programs
  • cGMP Training & Certification
  • RealTime™ Clinical Trial Oversight
  • Vaccine Development
  • Device & Combination Products

Our Partners: