The Regulatory Associate will report to the Senior Manager, Regulatory Affairs and, under the direction and guidance of the Associate Vice President, will help to ensure regulatory compliance of Prestige marketed products. Regulatory Affairs Associate (Tarrytown, NY). Assist with regu...
The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge...
The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge...
The Regulatory Associate will report to the Senior Manager, Regulatory Affairs and, under the direction and guidance of the Associate Vice President, will help to ensure regulatory compliance of Prestige marketed products. Assist with regulatory affairs projects and initiatives as needed, including ...
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 the Regulatory Affairs function by serving as an enterprise wide resource on public policy and IDR tre...
The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge...
JOB SUMMARY: The Regulatory Associate will report to the Senior Manager, Regulatory Affairs and, under the direction and guidance of the Associate Vice President, will help to ensure regulatory compliance of Prestige marketed products. Review product labeling for regulatory acc...
Job Description:Exciting opportunity to become an Associate at Credit Agricole Corporate and Investment Bank as part of the Regulatory Affairs team in New York, reporting to the CUSO Head of Regulatory Affairs. Within this context, your responsibilities will include:· Prepare, document, and re...
This role is responsible for the preparation of various regulatory Labeling submissions and as well as review of labeling documents for submission. Electronically search for new regulatory guidelines and regulations. Solid review, writing and communication skills and the ability to work independentl...
Stoneleaf Construction, LLC (“Stoneleaf”) is looking for an experienced Project manager to manage, supervise and oversee all site work in order to achieve project and company goals. The project manager’s main objective is to plan, budget, oversee and document all aspects of the spe...
The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures r...
This management position in Regulatory Affairs involves the ability to lead and manage a Therapeutic Area (TA) within Regenerons Regulatory Affairs organization so that all corporate objectives are met within specified timelines and so that the necessary state of compliance is maintained relative to...
The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge of regula...
In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents ...
In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents for ...
In addition, Senior Regulatory Affairs Associate is responsible for supporting a variety of activities in the department related to regulatory submissions and R&D requests, and supporting other departments within the organization. Ability to review regulatory and scientific submission documents for ...
The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures r...
Under oversight and direction from the Program Director, the GME Program Manager is responsible for the day to day administrative and operational management of the accredited/non-accredited residency/fellowship training program. The program manager functions in collaboration with the GME Office, Att...
Day-to-day management will include program operations, sales, renewals, program marketing, and regional coaching staff guidance. The focus of this position is to manage and grow Youth Program partnerships in Westchester County and Hudson Valley, NY. Youth Soccer Club Management – understanding of cl...
The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. Utilize regulatory expertise and knowledge of regula...
We are seeking a high-quality Program Manager to be a key partner in supporting the U. S Banks Program Management Office (PMO) manages cross-divisional, cross-product, and firm-wide initiatives on behalf of the U. The role is multi-faceted, offering the opportunity to lead, take ownership for, and c...
This management position in Regulatory Affairs involves the ability to lead and manage a Therapeutic Area (TA) within Regeneron’s Regulatory Affairs organization so that all corporate objectives are met within specified timelines and so that the necessary state of compliance is maintained relative t...
Squarespace is looking for a Payroll Specialist to join the Payroll function of our growing company. You will report to the Head of Global Payroll & Compliance. ...
Regulatory Affairs Certification (RAC) is a plus. Demonstrated expertise in preparing CMC sections of regulatory submissions (e. Strong understanding of global regulatory requirements, guidelines, and expectations related to CMC for pharmaceutical products (e. Experience with regulatory submissions ...
Being the primary point of contact for management regarding progress of project / program goals and ensuring effective and timely program-related communication across functional areas. Acquiring technical expertise in and managing existing systems and tools related to supporting tasks, projects, and...