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!
Medical Billing & Coding Specialist - NO CERTIFICATION REQUIRED We are seeking a Medical Billing & Coding Specialist to manage the revenue cycle for a busy orthopedic practice. This role is responsible for ensuring accuracy in coding, timely claim submissions, and...
...Ascendo Resources is working with a well-established, full-service law firm client that is seeking an experienced Legal Practice Assistant to support attorneys within its Commercial Real Estate practice in Charleston, SC. This full-time role offers the opportunity to...
...Experience working directly with people from diverse racial, ethnic and socioeconomic backgrounds Desired Skills: Associate's and/or Bachelor's Degree Bilingual (English and Spanish) Experience with clients dealing with substance use or temporary housing...
...approaches, and ensure scalability and performance. Coordinate with offshore teams by assigning tasks, tracking progress, and ensuring on-... ...position, subject to applicable eligibility requirements: ~ Medical / Life Insurance ~ Paid holidays ~ FSA & HSA ~ Commuter...
...:00pm - 10:30pm (Full Time, Swing) What Youll Make $20.60 - $21.86 per hour DOE/Credentials. An additional $3.00 per hour night shift differential will apply during the work hours of 10:00pm - 6:00am. Additional 5% Language Differential offered for Bilingual...