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!
...Brown & Brown is seeking an experienced Producer for its Personal Lines team in White Plains, NY . This position is responsible for promoting and executing on the sale of new and renewal business, providing and being a source of insurance expertise to customers...
...Curtiss Ryan Honda seeks a part time Parts Delivery Driver for our busy Parts department. Responsibilities include: daily parts pick up with cash and check transactions, shipping and receiving, and other miscellaneous duties. Applicant must be a very reliable, personable...
...Dynamic consulting firm is seeking a seasoned FSA to serve as a key member the healthcare actuarial team and support their clients' healthcare initiatives and innovations. Reporting to the Managing Director, this client-facing role will manage a diverse range of actuarial...
...Immediate need for a talented Web Developer / Front End Developer. This is a 06+months contract opportunity with long-term potential and is located in Charlotte, NC(Hybrid) . Please review the job description below and contact me ASAP if you are interested. Job...
...pharmacy networks that can serve Upward Health patients and their unique needs. Create, maintain, and update the clinical market resource directory in Salesforce as resources are added and/or discontinued. Prioritize network and directory building through both an...