CenExel CBH in Gaithersburg, MD seeks an entry-level Regulatory Affairs professional to organize and implement regulatory documents for FDA-guided clinical trials. You will maintain regulatory files, prepare submissions, and coordinate training per SOPs with IRB interfaces. Responsibilities include collecting sponsor documents, managing licenses and logs, and serving as a regulatory resource for the team; 0-2 years’ experience and proficiency in Excel/Word are required. #J-18808-Ljbffr Cenexelresearch
Job Description SummaryAt Novartis, we are reimagining medicine to improve and extend people's lives. Every day, our teams bring together innovative science, advanced technology, and a deep commitment to patients to help address some of the world's most challenging health...
...adequate steam or hot water production for user requirements in the entire system.You will assist in the operation and operational maintenance of multi-fuel power boilers and auxiliary equipment.You will utilize safety practices, rules, regulations, and procedures to...
...Novartis Pharmaceuticals Corporation seeks a Director to lead product strategy and governance for enterprise data foundations, including reference data, master data, metadata, and standards. You will define the vision, roadmaps, and adoption plans, partnering with the...
PepsiCo, Inc. - - Responsibilities: Load/unload trucks with forklift/pallet jack; Build pallets according to load sheets; Ensure accuracy with shipping/receiving documents; Shrink-wrap and stabilize pallets; Maintain clean, safe work environment
...With over 40 years of experience in Real Estate Law, McCabe, Weisberg & Conway, LLC has an immediate opening for a full-time Billing Clerk in our West Palm Beach, FL office! MWC is a high volume, fast-paced, multi-office law firm representing Mortgage Lenders, Banks and...