Regulatory Affairs Jobs in USA

Primary Function of Position:Serve as the primary regulatory representative on project and product core teams. The Regulatory Affairs Specialist works across the organization in supporting design control activities US and Canada regulatory assessment and submissions and liaises with global regulator...

This is a remote position with up to 50% domestic travel required. Candidates may reside anywhere in the United States.The HCV Associate Director Thought Leader Liaison (TLL) is national in scope and responsible for the strategic direction that uncovers and accelerates MAVYRET business results. This...

By joining Bio-Techne youll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne and all of its brands provides tools for researchers to further treat and prevent disease worldwide.Pay Range:Target Salary Range:...

Where Youll WorkHello HumankindnessImagine working in an environment where your experience and dedication truly makes a difference guided by Dignity Healths profound values: Dignity Justice Stewardship Collaboration and Quality. Here patient-first care isnt just a motto its our daily practice. As a...

Job Description SummaryThe Sr. Research Manager (RM) is responsible for development and execution of the research strategy and overall management of the research portfolio for the Ultrasound AI Center of Excellence which includes Caption Healthcare and Intelligent Ultrasound teams under our Advanced...

Department:107000 RegulatoryLocation:San Diego USA- RemoteBe a part of a global team that is inspired to make a difference in the lives of people living with rare disease.At Travere Therapeutics we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on...

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This is what you will do:The Clinical Study Administrator (CSA) assists in the coordination of study activities from the start up to execution and close out within Country Operations Management (COM) to ensure quality and consistency of trial deliverables to time cost and quality objectives accordin...

Job DescriptionOur market access team is passionate about bringing our medicines to patients around the world.As a member of the Sac-TMT/Womens Cancers team the Director Oncology Global Market Access will lead global access strategy development and execution for defined Sac-TMT indications within th...

The Senior Associate Regulatory Affairs Submission Management manages medium to high impact moderately complex submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams this individual establishes and maintains submission content planne...

The Senior Manager RA Global Reg Strategy US & Canada - Immunology is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. Assures that regulatory strategies defined wit...

The Senior Manager RA Global Reg Strategy US & Canada - Immunology is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. Assures that regulatory strategies defined wit...

The Associate Director Commercial Development Established Products drives commercial strategy and execution for the Authorized Generic portfolio. This leader identifies growth opportunities shapes lifecycle and portfolio strategies and mobilizes cross-functional teams to deliver revenue profitabilit...

As we scale rapidly in North America were building a world-class Public Affairs function to shape policy strengthen our regulatory positioning and elevate our influence across government academia and leading institutions.The RoleWere seeking a North America Lead Public Affairs to serve as IFSs prima...

The Director Regulatory Affairs Global Regulatory Lead (GRL II) Global Regulatory Strategy is responsible for developing and implementing global strategies to secure and maintain market approval for product(s) in the assigned therapeutic area. Leads the Global Regulatory Product Team (GRPT). Continu...

Remote Regulatory Affairs contractor requires: Bachelors degree in engineering life sciences regulatory affairs legal or a related field 5-10 years of global medical device regulatory experience Proven experience preparing writing and submitting FDA 510k submissions (end to end) Experience with oph...

Remote Regulatory Affairs contractor requires: Bachelors degree in engineering life sciences regulatory affairs legal or a related field 5-10 years of global medical device regulatory experience Proven experience preparing writing and submitting FDA 510k submissions (end to end) Experience with oph...

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...

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...

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...