Legislative Assistant Jobs in the United States
NYC Health
New York, NY
MetroPlusHealth provides the highest quality healthcare services to residents of Bronx, Brooklyn, Manhattan, Queens and Staten Island through a comprehensive list of products, including, but not limited to, New York State Medicaid Managed Care, Medicare, Child Health Plus, Exchange, Partnership in Care, MetroPlus Gold, Essential Plan, etc. With wide latitude for individual initiative and decision making, the Senior Director of Regulatory Affairs is responsible for providing leadership and oversight of the Regulatory Affairs unit relating to all products offered by MetroPlusHealth, as well as leading other projects assigned by Executive Leadership.
NYC Health
Manhattan, NY
Master’s degree from an accredited college or university in Accounting, Finance, Business Administration or a related discipline with an emphasis on accounting and financial systems; and two (2) years of responsible-level experience in fiscal management or administration with an emphasis on financial systems, management information and controls, one (1) year of which must have been in a responsible administrative or managerial capacity; or. Every employee takes a person-centered approach that exemplifies the ICARE values (Integrity, Compassion, Accountability, Respect, and Excellence) through empathic communication and partnerships between all persons.
NYC Health
Manhattan, NY
Master’s degree from an accredited college or university in Accounting, Finance, Business Administration or a related discipline with an emphasis on accounting and financial systems; and two (2) years of responsible-level experience in fiscal management or administration with an emphasis on financial systems, management information and controls, one (1) year of which must have been in a responsible administrative or managerial capacity; or . - Reviews operational procedures in compliance with authorized systems; implements changes necessary to stave off deterioration of their effectiveness and recommends and guides the installation of improved procedures for efficient operation of current health care setting financial systems.
NYC Health
Manhattan, NY
A master’s degree with a major in accounting, finance or business administration, with emphasis on accounting and financial systems from an accredited college or university; and five (5) years of responsible-level experience in fiscal management or administration with an emphasis in financial systems, management information and controls, of which at least three (3) years shall have been in a responsible supervisory, administrative or management capacity; or. The Finance Manager works under the general supervision of the Director of Fiscal Affairs, provides guidance to the PAC department personnel and is responsible for a full range of activities which ensure the operational effectiveness and excellence of the Post-Acute Care (PAC) business unit.
NYC Health
Manhattan, NY
A deep study and understanding of all NYC H+H managed care contracts and reimbursement policies and methodologies in order to identify and implement ways to appropriately maximize reimbursement and identify opportunities to optimize efficiencies for services rendered in inpatient care settings; Working with Revenue Cycle to develop a routine cadence in working with the UM vendors to understand and escalate managed care related payment issues to contracted payers and monitoring those issues to resolution; Establish and maintain efficient system-wide tools and methods to: 1) track and analyze revenue opportunities tied to inappropriate medical necessity denials, and 2) aid in implementing systemwide utilization management operations in conjunction with revenue cycle, quality and safety. Such workstreams may include: payer notification/preauthorization, concurrent review, extended stay documentation, discharge planning, and clinical appeal processes; Develop and maintain tools to track the changing federal and state regulatory landscape around utilization management and collaborate when requested in developing responses to proposed regulatory & policy changes that reflect NYC H+H position.
NYC Health
Brooklyn, NY
Master’s degree from an accredited college or university in Accounting, Finance, Business Administration or a related discipline with an emphasis on accounting and financial systems; and two (2) years of responsible-level experience in fiscal management or administration with an emphasis on financial systems, management information and controls, one (1) year of which must have been in a responsible administrative or managerial capacity; or. Under the general supervision of the Budget Director, with latitude for independent judgment, is responsible for the overall financial management of the Affiliation contract/budget as well as the creations, monitoring, and reporting on operational expenditures and revenue.
Avidity Biosciences
San Diego, CA
Utilizing its proprietary AOC platform, Avidity demonstrated the first-ever successful targeted delivery of RNA into muscle and is leading the field with clinical development programs for three rare muscle diseases: myotonic dystrophy type 1 (DM1), Duchenne muscular dystrophy (DMD) and facioscapulohumeral muscular dystrophy (FSHD). The Senior Director, Regulatory Affairs is responsible for establishing regulatory strategies in coordination with departmental leadership, and independently developing and managing life cycle plans along with regulatory submissions and approvals.
Avidity Biosciences
San Diego, CA
The role will include reviewing proposed promotional communications including labeling, advertising campaigns, digital and DTC marketing, corporate presentations and press releases, scientific communications and promotional exhibits to ensure compliance with regulations and company policies. Utilizing its proprietary AOC platform, Avidity demonstrated the first-ever successful targeted delivery of RNA into muscle and is leading the field with clinical development programs for three rare muscle diseases: myotonic dystrophy type 1 (DM1), Duchenne muscular dystrophy (DMD) and facioscapulohumeral muscular dystrophy (FSHD).
Axelon Services Corporation
Pittsburgh, PA
This includes gathering, maintaining and correcting data in to the SAP EHS database for the preparation of Safety Data Sheets (SDSs), preparation of data for regulatory reports, and responding to customer requests for information regarding regulatory compliance and products. Required Skills: Strong computer skills - advanced knowledge of Microsoft Office, other databases .
Axelon Services Corporation
Charlotte, NC
Assist in ensuring the accuracy of the daily jump off Regulatory Capital and MCS Target Ratios actuals for RRP, or results from scaling or estimate methodology in absence of daily Regulatory Capital and MCS Target Ratios. Ensure Regulatory Capital and MCS Target Ratios data accuracy are consistent with legal entity s financials, actuals and estimates for RRP purposes, including weekly/intra-month capital.
Axelon Services Corporation
Jacksonville, FL
Regulatory Control is responsible for establishing and maintaining control frameworks designed to manage regulatory, monitoring, surveillance, employee compliance, transaction monitoring and client screening. Ensuring operational discipline combined with regulatory risk awareness & investigative skills and warrants that workflows are governed by established policies, clearly defined processes, and escalation points.
Axelon Services Corporation
Oakland, CA
Working as part of a highly motivated and impactful team, the successful candidate will help the Wildfire Risk organization attain its goals by leveraging exceptional communication, analytical and strategic skills, while applying the highest work ethic, and has energy and passion for risk-informed, data-driven decision making, collaboration and continuous improvement. - Review and assist subject matter experts with development of testimony, work papers and discovery responses related to Wildfire Risk work, settlement documents and communications materials; anticipate and understand the impact and proactively address issues.
Axelon Services Corporation
Charlotte, NC
Ensure Regulatory Capital and MCS Target Ratios data accuracy are consistent with Basel III rules, actuals and estimates for RRP purposes, including weekly/intra-month capital . This Regulatory Reporting team lead analyst role is responsible for supporting the accurate and timely preparation and submission of regulatory reports to various constituencies based on applicable requirements such as U.S. Regulatory rules and instructions .
Rose International
Stamford, CT
Collaboration and Teamwork: Work closely with cross-functional teams including Product Development, R&D, Quality Assurance, and Legal to ensure accurate and timely completion of SDS authoring and GHS classification projects. • Independent Project Management: Independently manage projects related to SDS authoring and GHS classification, ensuring deadlines are met and deliverables are compliant with regulatory requirements.
CSL
King of Prussia, PA
Assure a productive collaboration with important team members, such as Regional commercial operations, to ensure successful development, strategic agreement and execution of regional regulatory strategies that result in successful applications for assigned products, from early development to Marketing Authorization (MA), and for any post MA submissions. Leading the establishment and maintenance of high-quality relationships with regional health authorities and collaborating with respective GRA Global Product Strategy (GPS) TA Leads & GRA CMC Site Leads to enhance these relationships.
CSL
King of Prussia, PA
In specific instances when serving as a Global Regulatory Lead (GRL) - EHT, acts as the primary regulatory interface for the GRAST, and supports GRL in relevant strategy/delivery teams (e.g., Product Strategy Team (PST), Clinical Development Team (CDT), Safety Management Team (SMT), Device Delivery Team, and Commercial Development. Cultivate and strengthen strategic relationships with members of the GRA functions and partners in global primary packing and medical devices (PPMD), product development (BPD/PPD), clinical pharmacology and pharmacometrics, clinical development, commercial strategy, safety, project management, quality and TALTs.
CSL
King of Prussia, PA
Responsibilities and accountabilities: Lead CTA activities for large and/or complex clinical trials during the entire study lifecycle: develop overall CTA concept and provide CTA strategic inputs during GRA TA meetings, SET meetings, GRAST meetings and during meetings with CRO. Coaches and trains lower level professionals through sharing of lessons learned, staying ahead of new CTA and regulatory trends and participate to opinion sharing as CTA experts in trade association in collaboration with the Global Regulatory Intelligence and Policy (GRIP) team.
CSL
King of Prussia, PA
You will be a member of the GRA Regional Leadership Team and contributes to the vision and goals for Global Regulatory Affairs (GRA) by: Provide leadership to the respective Regional Team, overseeing and accountable for all regional regulatory strategic and operational tasks for licensed products advertising and promotion requirements for all CSL departments. With operations in 35+ nations and ~ 30,000 employees worldwide, CSL is inspired to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza.