Are you a Regulatory Affairs professional looking to work independently and take ownership of the writing of CMC sections of DMF, BLA, and NDA submissions? Have you supported full product development activities from pre-clinical/clinical to FDA submissions? Are you interested in helping a company expand their client base in new countries? Do you have experience independently writing CMC sections of global regulatory submissions? This position could be for you!
If you're interested in a Lead Regulatory Affairs Specialist position with a well established pharmaceutical company in Madison, Wisconsin, apply here for more details!
...is an exciting opportunity to support key members of our leadership team and be involved in the dynamic growth plans for our North American business. In addition to core EA responsibilities, this role will also include maternity cover for a fellow Executive Assistant...
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At BayCare, we are proud to be one of the largest employers in the Tampa Bay area. Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than...
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...Tuesdays, Wednesdays, and Thursdays for collaboration and connection. Position Summary: The Finance Analyst assists the Sourcing Directors by providing financial analyses of supplier pricing proposals for a vast portfolio of generic pharmaceutical products. The...