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
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.
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
NOTE: Executive level applicants, please send cover letters and resumes directly to