Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. The Manager of Regulatory Affairs (RA) Labeling will assist in the development of a cross functional labeling strategy for products worldwide, including providing input on labeling requirements and strategic guidance duri

/JOB PURPOSE Manages all regulatory activities for new development programs, pre IND through BLA/NDA and post approval, with a particular focus on biologics (ADCs, bispecifics, and etc.). Responsible for developing and implementing global regulatory strategies encompassing clinical, non clinical and CMC disciplines, as well as companion diagnostics, as appropriate. Provide

Assist in the preparation of external reports, ESG disclosures, and surveys such as CDP, EcoVadis, S&P Global and others. Assist in the collection, analysis and management of data for ESG reporting frameworks and support work processes, policies, etc. Collaborate with various teams to address customer inquiries and requests related to ESG topics. Proactively identify oppo

The Policy Advisor is a key member of the policy team, reporting directly to the Policy Director. This role involves providing strategic advice, conducting in depth policy analysis, and assisting in the development and implementation of policies, initiatives, and strategic priorities for Montgomery County. The Policy Advisor plays a critical role in supporting decision ma

Site Name UK Hertfordshire Ware RD, Durham Blackwell Street, GSK House, USA Pennsylvania Upper Providence Posted Date May 2 2024 As Regulatory Manager for devices, you will manage the overall global regulatory and advocacy strategy for GSK's portfolio of combination product devices (injectable and inhalation) across modalities and lifecycle We create a place where people

Conduct pre claim investigation, legal research and initial case assessment Draft pleadings, motions and appellate documents and filing with the courts Prepare records, review and prepare exhibits, analyze medical records, and trial preparation Contact outside sources (government agencies, etc.) to obtain public information and review and analyze the same Search and retri

Collaborates in the development of communications strategies tailored for target audiences over multi channel platforms, and leads the execution of those efforts to inform, educate, and influence both internal and external audiences. Develops integrated communications strategies to reach key audiences, oversee implementation, and measure results. Develops message framewor

The FDA Center for Tobacco Products requires the assistance of minors ages 16 17 and those under age 18 20 to attempt the purchase of tobacco products from local tobacco retailers. The goal of the program is to ensure tobacco retailers are complying with Federal laws and regulations that prevent them from selling tobacco products to minors. This will be a part time, posit

Responsible for managing Med Legal Review (MLR) submissions for a variety of Pharma Brand companies, including submitting in MLR Systems Develop and maintain constant knowledge of pharmaceutical company requirements, including but not limited to system and regulatory guidance and annotation guidelines Partner with team leads to provide consultation to Account Managers on

As a combined organization, and is undertaking what is perhaps the central challenge of our times to help drive the transition to net zero carbon economies while ensuring that no working families, businesses, or local communities are left behind. To do that, we are the utility industry's top provider of turn key energy efficiency and grid optimization programs and product

Responsible for managing Med Legal Review (MLR) submissions for a variety of Pharma Brand companies, including submitting in MLR Systems Develop and maintain constant knowledge of pharmaceutical company requirements, including but not limited to system and regulatory guidance and annotation guidelines Partner with team leads to provide consultation to Account Managers on

#LI OD1 #LI Onsite CBIZ.Jobs Category Benefits & Insurance REASONABLE ACCOMMODATION If you are a qualified individual with a disability you may request reasonable accommodation if you are unable or limited in your ability to use or access this site as a result of your disability. You can request a reasonable accommodation by calling 844 558 1414 (toll free) or send an ema

#LI OD1 #LI Onsite CBIZ.Jobs Category Benefits & Insurance REASONABLE ACCOMMODATION If you are a qualified individual with a disability you may request reasonable accommodation if you are unable or limited in your ability to use or access this site as a result of your disability. You can request a reasonable accommodation by calling 844 558 1414 (toll free) or send an ema

FuturePlan is the nation's largest third party administrator (TPA) of retirement plans, partnering with advisors in all 50 states. FuturePlan delivers the best of both worlds high touch personalized service from local TPAs backed by the strength and security of a large national firm, Ascensus. Our roots go back decades, with nearly 30 outstanding legacy firms now joined t

Regulatory and Quality Assurance Specialist (Part time, 20 hrs/wk) Department Oticon Medical Other Job Locations US NJ Somerset Job ID 2024 21151 Overview This is a part time (20 hours/wk) position In this position you will be responsible for assuring quality and regulatory compliance including complaint handling for Oticon Medical LLC, as a US agent and initial importer