Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM

We are seeking a Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM to join our team. As a Sr Regulatory CMC Consultant, you will be responsible for providing regulatory support for small molecule and Veeva RIM projects. Responsibilities Good knowledge of North America regulatory affairs framework Understanding of requirements and processes to maintain a product on market, report, and surveillance Understanding of drug development and related concepts Ability to assess and understand regulatory guidelines Strong written and verbal communication skills Ability to work effectively within a team environment Ability to plan, prioritize and contribute to work and projects in systematic and efficient manner Requirements Bachelor's, Master's or PhD degree in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another life-science field Typically requires 8 years of experience in the pharmaceutical or biotech industry or in a related field, or the equivalent combination of education and experience Job Data by YubHub .