The Associate Director Regulatory Affairs, Advertising and Promotion is responsible for providing commercial regulatory strategy and leadership to enable the US business to meet its commercial needs i...

Position ResponsibilitiesLeadership responsibility for global regulatory strategy to support the development of biomarkers, companion diagnostic tests, digital health and other devices to enhance the ...

Under the direction of regulatory affairs management, the incumbent independently prepares and directs global regulatory affairs activities and provides regulatory guidance during drug development, ap...

Under the direction of regulatory affairs management, the incumbent independently prepares and directs global regulatory affairs activities and provides regulatory guidance during drug development, ap...

US Medical Device Regulatory Affairs experienceKey Competencies Experience in successfully leading teams; ability to broadly represent the regulatory functions on project teams within BMS and across a...

We are seeking a passionate and detail-oriented Scientific & Regulatory Affairs Associate to play a pivotal role in advancing our mission. By ensuring our products and solutions meet all regulatory re...

The Associate Director Regulatory Affairs, Advertising and Promotion is responsible for providing commercial regulatory strategy and leadership to enable the US business to meet its commercial needs i...

Associate Director, Regulatory Affairs (In Vitro Diagnostics & Companion Diagnostics). Associate Director, Regulatory Affairs (In Vitro Diagnostics & Companion Diagnostics). Ensure global development ...

Ten years previous experience in global regulatory affairs and regulatory submissions for drugs, preferably in oncology. Directs and prepares global regulatory affairs strategies and executes regulato...

Associate Director, Regulatory Affairs (In Vitro Diagnostics & Companion Diagnostics). Associate Director, Regulatory Affairs (In Vitro Diagnostics & Companion Diagnostics). US Medical Device Regulato...

Associate Director, Regulatory Affairs (In Vitro Diagnostics & Companion Diagnostics). Associate Director, Regulatory Affairs (In Vitro Diagnostics & Companion Diagnostics). Ensure global development ...

The Associate Director Regulatory Affairs, Advertising and Promotion is responsible for providing commercial regulatory strategy and leadership to enable the US business to meet its commercial needs i...

The Associate Director Regulatory Affairs, Advertising and Promotion is responsible for providing commercial regulatory strategy and leadership to enable the US business to meet its commercial needs i...

Ten years previous experience in global regulatory affairs and regulatory submissions for drugs, preferably in oncology. Directs and prepares global regulatory affairs strategies and executes regulato...

Associate Director, Regulatory Affairs (In Vitro Diagnostics & Companion Diagnostics). Associate Director, Regulatory Affairs (In Vitro Diagnostics & Companion Diagnostics). Responsible for understand...

Associate Principal Scientist, Regulatory Affairs. The Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceutical projec...

Associate Principal Scientist, Regulatory Affairs. The Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceutical projec...

Role: Regulatory Affairs Associate III Location: Clark, NJ Duration: Long Term Contract Rate: $40/hr. Job Description: Review formulas for compliance with local regulations, in particular for US and C...

Directs and prepares global regulatory affairs strategies and executes regulatory activities for Taiho Oncology, Inc. Ten years previous experience in global regulatory affairs and regulatory submissi...

Independently prepares and directs global regulatory affairs activities and provides regulatory guidance during drug development, approval and post-approval processes, in coordination with internal an...

The Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for leading the development and maintenance of global labeling documents (e. This role will be within Global R...

The Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for leading the development and maintenance of global labeling documents (e. This role will be within Global R...

Responsibilities:Provides strategic and operational leadership in advertising and promotion for the US market in accordance with business goals and objectives, FDA regulation, ICH guidelines, PhRMA gu...

Assist the Manager of Regulatory Affairs for facility registrations, renewals, and document submissions to regulatory agencies (eg Drug and Cosmetic listings, etc. Assist the Manager of Regulatory Aff...

The Associate Director Regulatory Affairs, Advertising and Promotion is responsible for providing commercial regulatory strategy and leadership to enable the US business to meet its commercial needs i...

The Associate Director Regulatory Affairs, Advertising and Promotion is responsible for providing commercial regulatory strategy and leadership to enable the US business to meet its commercial needs i...

Remote - Regulatory Affairs Associate. About the job Remote - Regulatory Affairs Associate. Drafts and updates work instructions relative to the Regulatory Affairs department.

The Regulatory Affairs Associate Manager supports Colgate’s Oral Care and Personal Care divisions. Manage regulatory activities to ensure compliance with FDA’s Modernization of Cosmetic Regulatory Act...

This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Reg...

This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Reg...

The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that...

The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that...

Provide US strategic regulatory guidance to facilitate efficient and compliant drug development and product maintenance. Provide analysis, advice and guidance on US regulatory strategies. Provide expe...

Provide US strategic regulatory guidance to facilitate efficient and compliant drug development and product maintenance. Provide analysis, advice and guidance on US regulatory strategies. Provide expe...

The Associate Director/Director, Regulatory Affairs - GDP, provides essential support to the Senior Director in overseeing regulatory activities related to Quality of Life (QOL) initiatives on a regio...

Responsible for understanding the regulatory landscape, assessing regulatory risk, and developing global filing strategies. Ensure global development plans will meet global regulatory requirements by ...

Ensure global development plans will meet global regulatory requirements by soliciting and integrating regional regulatory strategy liaison input. US Medical Device Regulatory Affairs experience. Resp...

Responsible for understanding the regulatory landscape, assessing regulatory risk, and developing global filing strategies. Ensure global development plans will meet global regulatory requirements by ...

The Associate, Regulatory Affairs will work with Regulatory Counsel in regulator and entity relationships, cover important legislative and regulatory hearings and meetings as assigned, and supports th...

The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Utilize regulatory expertise and knowledge of regulatory requirements and r...