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!
Oversee daily distribution center operations to ensure efficient, productive, and safe performance, while meeting customer service and business objectives. Maintain optimal functionality of facilities and equipment, and ensure compliance with corporate and regulatory directives...
...or DO with an active, unrestricted medical license in the state of Indiana. Board certification (or eligibility) in Internal Medicine, Family Medicine, or a related specialty preferred. Previous experience in clinical trials, particularly as a Sub-Investigator...
...Behavior Analysis and Applied Behavior Analysis Strong Communication abilities and Behavioral Intervention skills Background in Psychology or related field Excellent observational and analytical skills Ability to engage with children and families in a...
...information by interviewing patient; reviewing and/or recording medical history; taking vital signs; confirming purpose of... ..., Planning, Dependability, Medical Teamwork. Medical assistants must be CMA (AAMA) certified or equivalent.~This position requires a high school...
...information Conduct quantity take-offs and pricing for all construction divisions Prepare and maintain a directory of suppliers, contractors, and subcontractors Create detailed and organized bid packages and participate in the bidding process Review and update...