Craig Claussen

Craig Claussen, Ph.D., RAC, is an accomplished regulatory affairs professional with extensive experience in regulatory CMC across various companies in the pharmaceutical and biotechnology sectors. Currently serving as Senior Director of Regulatory CMC at Global Regulatory Writing & Consulting, Craig Claussen has held significant positions at BlueRock Therapeutics as Director of Regulatory Affairs CMC, and at AbbVie in roles such as Associate Director of Regulatory Affairs for Oncology and CMC pertaining to biologics and gene therapy. Previous experience includes managerial responsibilities at Medline Industries as Senior Regulatory Affairs Specialist and QA Specialist, as well as a senior compliance role at ProPharma Group on assignment at Hospira.