Mr. Gottlieb graduated with a B.A. in Environmental, Population and Organismic Biology (EPOB) from the University of Colorado at Boulder in August of 2005. While studying at CU, Mr. Gottlieb was awarded a grant for undergraduate research, which he used to conduct a study on plant defensive chemistry. Mr. Gottlieb began his career in the biotech industry by working as an intern for CBR International Corp. during his final semester of college.

After graduation, Mr. Gottlieb began his professional career in Clinical and Regulatory Affairs at CBR International Corp. where he has gained training in auditing clinical trials, Good Clinical Practices, submission preparation, database management and Sponsor/FDA interactions.

Since joining the CBR team, Mr. Gottlieb has served in a variety of capacities. In addition to providing administrative assistance he has served as regulatory support for several different projects. Mr. Gottlieb provides technical writing assistance for in-house systems and management. In addition to performing on-site clinical audits, Mr. Gottlieb is also proficient in regulatory submission preparation from pre-IND requests to IND Amendments and annual reports.

With Mr. Gottlieb and other CBR International Corp. associates, CBR can offer the services of high quality professionals that work as a team to address specific client program issues in a highly cost effective manner. For a comprehensive assessment of your program requirements, please contact us by calling (720) 746-1190 or by email at info@cbrintl.com.