Regulatory Affairs Jobs in USA

1. Support regulatory submission and strategic direction for all ORICs development programs. 2. Lead to deliver high quality and timely regulatory submissions in alignment with corporate goals and in compliance with all applicable regulatory requirements.3. Coordinate and collaborate regulatory acti...

At Syngenta our goal is to build the most collaborative and trustworthy team in agriculture providing top-quality seeds and innovative crop protection solutions that improve farmers success. To support this mission Syngentas Regulatory Affairs Team is seeking a Regulatory Manager in Greensboro NC US...

Apex Clean Energy is seeking an experienced and strategic Vice President Transmission & Grid Strategy to lead the companys transmission planning interconnection grid integration and transmission analytics functions across its growing portfolio of utility-scale renewable energy energy storage and eme...

Regulatory Affairs Project Manager US Remote BasedFortrea is seeing a seasoned Project Manager with experience aligned with primary work in regulatory space. This role is accountable for communicating updates and issues to the team members as well as meeting the established timelines. The Regulatory...

Job Title: Senior Director Regulatory Affairs Strategy - Cell and Gene Therapy Introduction to role: Are you ready to set the global regulatory vision for pioneering cell and gene therapies and turn breakthrough science into real options for patients This role leads high-impact programs across cance...

IDEXX defines innovation in the industries we serve with a world-class product portfolio and an impressive pipeline focused on the this role as Senior R&D Manager New Product Development & Regulatory Licensing you will lead a team of talented scientists through the development and regulatory licen...

IDEXX defines innovation in the industries we serve with a world-class product portfolio and an impressive pipeline focused on the this role as Senior R&D Manager New Product Development & Regulatory Licensing you will lead a team of talented scientists through the development and regulatory licen...

Job SummaryThe Associate Director of Pediatric Clinical Research Cancer Center serves as the senior operational and execution leader for all pediatric cancer clinical research activities within the Cancer Center including early phase (Phase I/first in child) investigator initiated cooperative group...

At Alcon were passionate about enhancing sight and helping people see brilliantly. With more than 25000 associates we innovate fearlessly champion progress and act swiftly to impact global eye health. We foster an inclusive culture recognizing your contributions and offering opportunities to grow yo...

About the unitWith 2 floors and 165 beds we are able to provide care for long term care residents and post-acute rehab patients. Nurse-patient ratios vary depending on the shift and the population you will be serving. It has a long term care unit and a rehab unit. Each floor has designated units tha...

About the unitWe are able to provide care for post-acute rehab patients . Nurse-patient ratios vary depending on the shift and the population you will be serving. The facility focuss on patient specialties such as neuro rehab traumatic brain injuries amputations heat failure spinal cord injuries and...

SUMMARY/JOB PURPOSEThis role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data particularly serious adverse events (SAEs). This role provides support for all major tasks and oversight of outsourced vendors related to the management and best util...

Job Description About Allogene:Allogene Therapeutics with headquarters in South San Francisco is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. Led by a management t...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines. Our 115000 collea...

About This RoleAs a Scientist II within Pharma Validation Transfer and Registration (VTR) you will serve as a subject matter expert supporting analytical method validation transfer investigation and regulatory filings for small molecule and antisense oligonucleotide (ASO) products. This role partner...

SUMMARY/JOB PURPOSE: Provides leadership to the biostatistics function and direct management of biostatistics staff in developing statistical strategy design and analyses for clinical trials for multiple compounds with a focus on early phase (1/2) trials. Sets direction for statistical support of tr...

Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our Companys Oncology medicines span all phases of clinical development (pre-clinical to post-licensure)....

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

About the TeamThe Targeted Lipid Nanoparticle (tLNP) drug product development group within AbbVies tLNP CMC team is committed to advancing clinical-stage tLNP assets from First-in-Human (FIH) through Phase 2. The team collaborates across biologics discovery CMC partners Clinical Operations Regulator...

Hi were Oscar. Were hiring a Analyst Regulatory Affairs to join our Regulatory Affairs team.Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on serving our members. We started Oscar in 2012 to create the kind of health insurance company...