Regulatory Associate Jobs in USA

Your work will change lives. Including your own.The Impact Youll MakeLead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications.Influence the regulatory strategy of Recursions development prog...

Your work will change lives. Including your own.The Impact Youll MakeLead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications.Influence the regulatory strategy of Recursions development prog...

At Alcon were passionate about enhancing sight and helping people see brilliantly. With more than 25000 associates worldwide we innovate fearlessly champion progress and act with speed to advance global eye health. At Alcon youll be recognized for your contributions supported by an inclusive culture...

Classification Title:Postdoctoral AssociateClassification Minimum Requirements:Postdoctoral AssociateThe appointee shall have received the doctorate in a field appropriate to the assigned duties and responsibilities.Job Description:The Risk Assessment Core is seeking a highly motivated postdoctoral...

Welcome to Haleon. Were a purpose-driven world-class consumer company putting everyday health in the hands of just three years since our launch weve grown evolved and are now entering an exciting new chapter one filled with bold ambitions and enormous opportunity.Our trusted portfolio of brands i...

DescriptionJob Duties: Associate Regulatory Reporting - Trade Level with Goldman Sachs Services LLC in Dallas Texas. Responsible for preparing and submitting regulatory reports to agencies such as FINRA and the SEC ensuring compliance with global regulatory requirements. Analyzing large datasets to...

DescriptionJob Duties: Associate Regulatory Reporting - Trade Level with Goldman Sachs Services LLC in Dallas Texas. Responsible for preparing and submitting regulatory reports to agencies such as FINRA and the SEC ensuring compliance with global regulatory requirements. Analyzing large datasets to...

DescriptionDo you wantto be part of building a fully integrated biopharmaceutical company together with a team of highly skilled colleagues who are passionate about developing best-in-class therapeutics that address significant unmet medical needs Then Ascendis Pharma is committed to support your pe...

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The companys RAS(ON) inhibitors daraxonra...

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 Acadia PharmaceuticalsAcadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinsons d...

Job Title: Clinical Regulatory Writer Associate Director / ManagerLocation: Gaithesrburg MD- Hybrid (3 days onsite)Introduction to role:Are you ready to be part of the solution turning drug development strategies into reality As an Associate Director in Clinical Regulatory Writing youll play a pivot...

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together we support innovation from concept to commercialization offering expertise in regulatory strategy clinical tria...

Position Details: Our client a world-leading Pharmaceutical Company is currently looking for a Supplier Quality Engineer to join their expanding team. Job Title: Supplier Quality Engineer / Pharma External Manufacturing / Remote Work Duration: 6 months contract extendable up to 48 months Loca...

EDP Renewables is a global leader in the renewable energy sector and the fourth-largest wind energy producer. With a sound development pipeline first-class assets and market-leading operating capacity EDPR has undergone exceptional development in recent years and is currently present in 28 markets.O...

Career CategoryRegulatoryJob DescriptionJoin Amgens Mission of Serving PatientsAt Amgen if you feel like youre part of something bigger its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.Since 1980 weve helped pioneer the world of biotech in o...

The Associate Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. The Associate establishes and maintains submission content planners and associated timelines facilitates tactical submission team m...

The Associate Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. The Associate establishes and maintains submission content planners and associated timelines facilitates tactical submission team m...

DescriptionJoin a high-visibility Regulatory and Business Conduct Programs team role that protects Commercial Banking by owning FINRA licensing/registration controls control monitoring and critical reporting. Partner across Operations Risk Compliance and Technology to deliver data-driven insights an...

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...