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!
...Work from Home Data Entry & Office Administration Remote Online Role About the Job We are seeking motivated individuals in Shreveport... ..., technology, and Amazon . Flexible scheduling allows part-time or full-time work to suit your availability. Job...
...Credit Analyst, Credit & Lending Deal Packaging & Lender Outreach Custom Capital Remote... ...-quality Absolute NNN (triple net lease) investment opportunities nationwide.... ...requirements for the property they plan to purchase. Prepare Lender Presentations: Create...
...operations, installation, and/or maintenance for local off-site and/or remote locations. Instructs, directs, and checks the work of... ...Locations 2883 River Haven Rd, Clendenin, WV, 25045, US Travel Requirements Up to 50% Relocation Assistance Not currently offered...
...Note: Need Pharma and Consulting exp. Job Summary: We are seeking a highly skilled and experienced Launch Project Manager to join our dynamic organization. This role is integral to the successful introduction of new commercial brands and assets, ensuring that each...
...client service within a fast-paced, technology-driven environment. Interns work closely with our Client Advisory team to support active... ...multiple tasks in a deadline-driven environment Interest in legal services, research, or professional consulting preferred Additional...