Strategic Development and Representation for
Biotech, Device, and Pharmaceutical Companies

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

Current Opportunities at CBR International:

Director of Regulatory Affairs
The Director of Regulatory Affairs will be responsible for the leadership and oversight of the Regulatory Affairs Department and a staff of 6 to 10 professionals. The Director will be responsible for the day-to-day planning and oversight of all consulting assignments and client deliverables from CBR Regulatory staff as well as development and maintenance of CBR Regulatory Systems. This position has a career progression to Senior Director of Regulatory Affairs and Vice President of Regulatory Affairs. Competitive salary and benefits.

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

Clinical Affairs Associate – Associate's or Bachelor's; focused on support for clinical trials and trial documentation.

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

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


We are Expanding and We're Hiring!
CBR is growing! We have numerous opportunities for professionals at all levels.

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:


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