Meet Recruitment Limited
Senior Director Regulatory Affairs
Meet Recruitment Limited, California, Missouri, United States, 65018
Senior Director, Regulatory Affairs (Generalist)
Remote Position for West Coast-based candidates, frequent travel to Bay Area requiredMeet is partnering with a late-stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical Regulatory and Regulatory CMC functions. Our client recently reported positive P3 data for their lead drug candidate and is in the process of filing an NDA this year.Key Responsibilities:Carry out Reg Strategy and Reg CMC functions to support major Regulatory submissionsServe as a cross-functional leader within the organization to facilitate prompt and accurate regulatory documentationKey Qualifications/Requirements:12+ years of Regulatory Affairs (mix of Clinical Reg and Reg CMC highly preferred)NDA/late stage experience highly preferredNon-oncology experience required, rare disease preferredStartup experience highly preferredPlease feel free to reach out directly to
brandon@peoplewithchemistry.com
to discuss the details further!Seniority Level
DirectorEmployment Type
Full-timeJob Function
Quality Assurance, Project Management, and Accounting/AuditingIndustries
Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care
#J-18808-Ljbffr
Remote Position for West Coast-based candidates, frequent travel to Bay Area requiredMeet is partnering with a late-stage pediatric rare disease startup looking for a high-level Regulatory Affairs professional to join their team. This position will be reporting into the SVP of Regulatory Affairs and will be supporting Clinical Regulatory and Regulatory CMC functions. Our client recently reported positive P3 data for their lead drug candidate and is in the process of filing an NDA this year.Key Responsibilities:Carry out Reg Strategy and Reg CMC functions to support major Regulatory submissionsServe as a cross-functional leader within the organization to facilitate prompt and accurate regulatory documentationKey Qualifications/Requirements:12+ years of Regulatory Affairs (mix of Clinical Reg and Reg CMC highly preferred)NDA/late stage experience highly preferredNon-oncology experience required, rare disease preferredStartup experience highly preferredPlease feel free to reach out directly to
brandon@peoplewithchemistry.com
to discuss the details further!Seniority Level
DirectorEmployment Type
Full-timeJob Function
Quality Assurance, Project Management, and Accounting/AuditingIndustries
Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care
#J-18808-Ljbffr