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This is the entry level MSL position in which the individual contributor will learn and develop the capabilities and responsibilities of the role as defined by AbbVie Medical Affairs. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
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The Global Scientific Affairs COVID & Flu Senior Manager will play a key role in delivering in-house RWE projects and support the development of Vaccines and Antivirals strategy to keep up with the evolving RWE landscape.
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Managing on-site event set-up;•Advancing and staffing events hosted by third parties at which the Attorney General appears;•Traveling throughout the state and nationally to advance the Attorney General’s trips;•Working closely with press and intergovernmental affairs teams and the Attorney General’s security detail; and•Liaising with venue managers, vendors, other government agencies, community members, and stakeholders as appropriate for event planning and production.
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We apply our unique expertise in strategic communications, public affairs, research, and digital marketing to create sophisticated and customized strategies that make change possible for American and European clients.
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Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP development, and GMP audits and inspections). Minimum five (5) years of experience in Regulatory Affairs.
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Education: Bachelor degree required; MBA or Master degree in finance, international affairs or business administration a plus. Reporting Relationships: Sr Director, Credit and Political Risk - E&S and Specialty or VP, Credit and Political Risk – E&S and Specialty.
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Strong experience in end-to-end R&D Product Lifecycle Management solutions in configuration, development, and implementation, including integration across R&D functional disciplines (e.g. Product Development, Formulation, Regulatory Affairs, Food Safety, Supplier Quality Assurance, Packaging, etc.
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We are seeking a highly skilled Senior Manager, Regulatory CMC to join our Regulatory Affairs team. Minimum of 6+ years of experience in regulatory affairs with a focus on CMC within the life sciences.
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Sr. Manager/Dir of Policy & Regulatory Affairs| NJ,NY,PA | $165,000 - $175,000 + Bonus. The Senior Manager/Director of Policy and Regulatory Affairs will be responsible for managing the company's relationships and policy positions at PJM, federal and state regulatory agencies, and state legislative bodies.
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This position is for a legal affairs attorney who is responsible for independently handling the drafting and negotiation of legal terms for a variety of production and licensing agreements for the development, production and distribution of documentary and non-scripted reality television programming, as well as the drafting of agreements for on camera talent (e.g., hosts, experts, narrators, families, celebrities, etc.
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The Enterprise Services Business Risk Office provides risk management support to several lines of business including: Tech, Digital, Brand, Enterprise Supplier Management, Capital One Ventures, External Affairs, Capital One Software (COS) and Enterprise ML. We are on the cutting edge of risk management and provide support for new and emerging technologies as well as critical business strategies.
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Working in conjunction with the medical affairs and clinical development teams, evaluate potential external clinical research collaboration opportunities and facilitate the conduct of external clinical investigator-initiated trials (IITs) and company-sponsored trials.
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Foster robust cross-functional partnerships (Product Development, Marketing, Sales, Medical Affairs, Finance, Operations) to ensure strategic alignment and smooth commercialization. Foster robust cross-functional partnerships (Product Development, Marketing, Sales, Medical Affairs, Finance, Operations) to ensure strategic alignment and smooth commercialization.
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Interacts with Regulatory Affairs, and Manufacturing to ensure that regulatory submissions meet domestic and international standards and regulatory requirements. The QA Manager/Senior Manager will be responsible for the leadership and oversight of the Quality Systems at KTG. This individual will be required to provide subject matter expertise support across both GMP and GCP organizations.
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Assists in managing government affairs across Resolution Life Group. Experience managing government affairs a plus. 6+ years of experience with (i) corporate governance in a complex organization and (ii) reinsurance and mergers & acquisitions in the life insurance industry.
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affairs job Title: sr in Brooklyn, NY
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