Job Description. Mammoth BioSciences. OPPORTUNITY. Mammoth is hiring a Director/Sr. Director, Regulatory Affairs, Therapeutics, to lead the regulatory acti...
more
Position Summary Odyssey Systems has an exciting new opportunity for a Senior Program Manager supporting the Space Systems Command (SSC) International Affa...
more
Eagle Harbor, LLC, a subsidiary of Three Saints Bay, LLC, and a Federal Government Contractor industry leader, is seeking a Program Manager to manage our P...
more
SUMMARY/JOB PURPOSE. Responsible for creating, updating, and maintaining product information and labeling documentation for all relevant Exelixis products ...
more
SUMMARY/JOB PURPOSE. Responsible for managing and maintaining existing investigational new drug (IND) and clinical trial application (CTA) submissions and ...
more
JOB DESCRIPTION. You're an original. So are we. We're a company of people who like to forge our own path. We invented the blue jean in 1873, and we reinven...
more
SUMMARY/JOB PURPOSE. Support the early-stage pipeline by working across the Medical Affairs sub-functions, including the Medical Communications, Medical In...
more
Please contact Abdul on "" OR email me at "". Perform the coordination and preparation of regulatory submissions for brachytherapy devices and software dev...
more
Description. Key Responsibilities. Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission b...
more
Summary. The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products. Key Res...
more