Sanofi is Hiring a Regulatory Affairs Specialist Team Lead (contract) Near Bridgewater, NJ
Title: Regulatory Affairs Specialist Project Lead Work Schedule: 1st shift 8am-5pm Mon-Fri Location: Bridgewater, NJ - 100% remote Contract Length: 5 Months 27 days possibility to extend Sanofi's contingent workforce program, FLEXT Direct, is seeking a Regulatory Affairs Specialist Project Lead for an 5 month 27 day contract. DescriptionThis role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. Additionally, this role leads the development of a global HA (Health Authority) interaction plan and strategy in collaboration with GRT (Global Regulatory Team) and is accountable for the communication of the key outcomes to senior management. Top 3 Must Have
Leadership capabilities and ability to work with cross-functional team
Knowing when to escalate concerns
Regulatory Experience, 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development Top
Nice Skills
Advanced Degree
Filed marketing application (strong plus before)
Experience
At least 8-10 years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development.
Education
BS/BA degree in a relevant scientific discipline required. Advanced degree (PharmD, PhD, MD or DVM or MSc in Biology, Life Science, or related field) is preferred.