- Spectraforce Technologies Inc (Bridgewater, NJ)
- Job title: CMC Regulatory Technical Writer II Location: Bridgewater, NJ, Hybrid Duration: 1 year SHIFT SCHEDULE 1st shift, 9-5 EST Mon-Fri Pay Rate starts: $47/ ... in Microsoft Office (Word, Excel, PowerPoint) VEEVA experience is a plus Description: The CMC Regulatory Technical Writer II authors high quality Module 2 and 3… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …personnel in other departments including Marketing, CMR, Legal, and counterparts in NNAS Regulatory Affairs . Has a positive approach to work projects and ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...tasks and assignments Participates in department forum meetings eg CMC , PRB, and ensures that proper minutes from these… more
- Integrated Resources, Inc (Atlanta, GA)
- Job Title: Regulatory Affairs Specialist Project Lead I Location: Washington DC, DC (Fully Remote) Duration: 06 months + Part-Time Role- (Mon - Fri 9 AM - 1 ... in a pharma regulatory -related role open all therapeutic areas (not manufacturing), non- CMC experience * Open to previous Sr. or Leadership exp * Fluent with… more
- Bausch + Lomb (Bridgewater, NJ)
- …the advancement of eye health in the future. **Objectives/Purpose of Job:** + The Regulatory Affairs Senior Specialist handles US regulatory development ... Regulatory Authorities for assigned products. + Liaise with country-specific regulatory affairs personnel for international submissions and registrations. +… more
- Kedrion Biopharma, Inc. (Fort Lee, NJ)
- …Responsible for US change control assessment for assigned products. + Manage regulatory affairs activities including preparation of Annual Report, Change Control ... required, and the role will collaborate with tasks across the existing US Regulatory Affairs team Education/Experience: + BS/BA/MS degree in science. Minimum of… more
- Novo Nordisk (Plainsboro, NJ)
- …personnel in other departments including Marketing, CMR, Legal, and counterparts in NNAS Regulatory Affairs . Has a positive approach to work projects and ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...and assignments + Participates in department forum meetings eg CMC , PRB, and ensures that proper minutes from these… more
- Sanofi Group (Bridgewater, NJ)
- …of the Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Specialist leverages their regulatory ... pharmaceutical/biotechnology industry experience, including at least 4 years of relevant Regulatory Affairs experience (regionally and/or global) especially in… more
- Rush University Medical Center (Chicago, IL)
- …and coding. Certifications may include Certified Professional Coder (CPC), Certified Coding Specialist (CCS) and Certified Medical Coder ( CMC ), and any other ... communicates with Revenue Cycle colleagues, study teams, patients, Office of Research Affairs , IRB, RUMC Compliance, and all partners in the Research Continuum. *… more
