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Proposals to allow the cheap kamagra jelly federal government to negotiate prescription drug prices, such as kamagra oral jelly best price H.R. 3, the Elijah E. Cummings Lower Drug Costs Now Act, aim to lower out-of-pocket drug costs for Medicare beneficiaries and kamagra oral jelly best price private plan enrollees and achieve savings for Medicare.

The debate over a budget reconciliation package in the coming weeks, and possibly months, is likely to focus heavily on the savings to Medicare, which can be used to expand Medicare benefits and fund other health care priorities. However, by lowering Medicare spending kamagra oral jelly best price for Part D, which covers retail prescription drugs, drug price negotiation proposals would also be expected to lower premiums that beneficiaries pay for Part D coverage.According to an analysis by Medicare’s actuaries of the version of H.R. 3 that passed the House of Representatives in the 116th Congress, the drug price negotiation provisions in the legislation would reduce spending by Medicare Part D enrollees by $117 billion between 2020 and 2029, including a reduction of $102.6 billion in cost sharing for people who use drugs covered under Part D that are subject to negotiation, and another $14.3 billion reduction in Part D premiums (in addition to Medicare savings).

This data note estimates average premium savings attributable to the negotiations kamagra oral jelly best price provision of H.R. 3 on a per capita basis for Part D enrollees who pay premiums (including those receiving partial low-income subsides) in dollar amounts and as a share of the base beneficiary premium, based on aggregate premium reductions and baseline premiums projected by Medicare’s actuaries through 2029.How does drug price negotiation affect Part D premiums?. Under Part D, beneficiary premiums are calculated to cover 25.5 percent of costs for standard coverage, kamagra oral jelly best price which includes benefit payments before the catastrophic coverage threshold as well as catastrophic costs (i.e., reinsurance).

Allowing the federal government to negotiate drug prices is expected to result in lower drug prices for those drugs subject to negotiation, which would lower Medicare spending for the standard drug benefit and lower Part D premiums, with significant reductions in reinsurance spending (i.e., costs above the catastrophic threshold). These reductions are expected to be somewhat offset by cost increases attributable to a reduction in rebates paid by drug manufacturers to Part D plans (which plans use to lower their total costs) and higher kamagra oral jelly best price prices for new drugs.What is the expected magnitude of savings on Part D premiums per enrollee?. Under drug price negotiation, premium savings for Medicare beneficiaries are projected to increase from an estimated 9% of the Part D base beneficiary premium in 2023 to 15% in 2029.

Medicare’s actuaries have estimated that the Part D base beneficiary premium, which covers the cost of basic Part D coverage, will increase from around $440 per year in 2023 to around $560 in 2029. The $14 billion in aggregate Part D premium savings from drug price negotiation over a decade translates into estimated per capita savings for Part D enrollees who pay premiums of $39 annually in 2023, increasing to $85 annually in kamagra oral jelly best price 2029 (Figure 1). This translates to savings of 9% of the base beneficiary premium in 2023 and 15% in 2029.

These estimates may understate premium savings kamagra oral jelly best price for Medicare beneficiaries that could be achieved under the current version of H.R. 3, which requires the Secretary to negotiate prices for a larger number of drugs in year 2 than the prior version of H.R. 3 that the actuaries kamagra oral jelly best price analyzed.

In addition, savings could be higher or lower than our estimates depending on the actual base beneficiary premium each year as well as premiums for plans that beneficiaries enroll in, which vary widely each year from the base premium amount. These estimates also do not reflect kamagra oral jelly best price the interactive effects of other provisions in H.R. 3, such as the Part B and Part D inflation caps or Part D benefit redesign, which would also affect beneficiary premiums and cost sharing.This work was supported in part by Arnold Ventures.

We value our funders kamagra oral jelly best price. KFF maintains full editorial control over all of its policy analysis, polling, and journalism activities.The high cost of prescription drugs continues to be a top health priority for the public. Policymakers at kamagra oral jelly best price the federal and state level are pursuing a range of options to lower drug prices for Americans, one of which would allow for the safe importation of prescription drugs from Canada and other countries, based on evidence showing that people often pay more for medications in the U.S.

Than elsewhere. In an executive order issued July 2021, President Joe Biden directed the Food and Drug Administration (FDA) to work with states to import prescription drugs from Canada, an approach that was put into place by the previous Administration and has bipartisan support among the general public (Figure 1).Figure 1. Majority of the Public Favors Allowing kamagra oral jelly best price Americans to Buy Prescription Drugs Imported from CanadaThese FAQs discuss recent efforts related to prescription drug importation, the history of this approach, challenges that previous efforts to carry out importation proposals have faced, and stakeholder views.1.

What is the current status of prescription drug importation?. Current law allows for the importation of certain drugs from Canada under defined, limited circumstances, and only if the Secretary of the United States Department of Health and Human Services (HHS) certifies that importation poses no threat kamagra oral jelly best price to the health and safety of the American public and will result in significant cost savings to the American consumer. In September 2020, the Trump Administration issued a final rule and final FDA guidance, creating two new pathways for the safe importation of drugs from Canada and other countries, and then-HHS Secretary Alex Azar certified that importation of prescription drugs poses no risk to public health and safety and would result in significant cost savings.Soon after the rule was finalized, PhRMA and other parties filed a lawsuit challenging the rule based on safety and other concerns.

In May 2021, the Biden Administration sought to dismiss this lawsuit, arguing that plaintiffs cannot show the final rule or the certification by the HHS Secretary kamagra oral jelly best price has harmed them. Because the FDA has not authorized any state importation plan under the final rule, and there is no timeline for authorization, the Administration asserts that “possible future injuries to Plaintiffs’ members are overly speculative and not imminent.” The federal court has not yet responded to the Administration’s motion to dismiss the lawsuit.The Biden Administration’s position on this lawsuit has opened the door for states to move forward with drug importation plans, as discussed further below, and President Biden’s recent executive order directly instructs the FDA to work with states to import prescription drugs from Canada.2. Why is importation of prescription drugs from Canada being considered kamagra oral jelly best price as a way to lower drug costs in the U.S.?.

Many studies have shown that people in the United States often pay more for their prescription drugs than in other developed countries, including Canada. According to kamagra oral jelly best price one analysis of a subset of single-source brand-name drugs, Canadian drug prices are about 28% of the price in the United States, while another analysis of a broad range of drugs found that Canadian prices are 46% of those in the United States.Canada’s drug prices are generally lower than those in the United States because the Canadian government has various mechanisms to lower the cost of prescription drugs. Since 1987, the Patented Medicine Prices Review Board (PMPRB) has regulated the price of patented (i.e., brand-name) drugs in Canada to ensure that they are not excessive.

The PMPRB reviews the prices charged for drugs, and if the Board determines the price of a drug is excessive, it can order a patentee to lower the price of a drug, including requiring a monetary payment kamagra oral jelly best price for the excess revenue earned from the drug.3. How does current U.S. Law regulate the importation of prescription drugs from other countries?.

In order for a drug to be marketed in the United States, it must first receive FDA approval and meet standards set forth in the kamagra oral jelly best price Food and Drug Cosmetic (FD&C) Act of 1938. Any drug that is “unapproved,” meaning it does not meet these standards, is not eligible for importation. Currently, the only type of legally imported drugs kamagra oral jelly best price are those that are.

1) manufactured in foreign FDA-inspected facilities, the subject of an FDA-approved drug application, intended for use by U.S. Consumers, and imported kamagra oral jelly best price into the U.S. By the drug manufacturer, and 2) those that are U.S.-approved and manufactured in the U.S., sent abroad, then imported back into the U.S.

Under rare circumstances such as for emergency medical purposes or in the case of kamagra oral jelly best price product recalls. These importation regulations pertain only to the drug product itself, and are not related to the cost of imported products.In 2000, Congress enacted the Medicine Equity and Drug Safety (MEDS) Act, which added Section 804 to the FD&C Act, to allow pharmacists and wholesalers to import prescription drugs directly from certain industrialized countries, including Canada, subject to specified limitations and safeguards. The MEDS Act allows such importation, subject to an important kamagra oral jelly best price requirement.

To do so, the HHS Secretary must demonstrate that the program. €œposes no additional risk to the public’s health and safety,” and “results in a significant reduction in the cost of covered products to the American consumer.”The Medicare Modernization Act of 2003 (MMA) amended the Section 804 importation kamagra oral jelly best price language that was added by the MEDS Act. The MMA specifies that wholesalers and pharmacists can only import prescription drugs from Canada, not other industrialized countries.

The MMA also authorizes the Secretary to terminate such importation programs if they do not meet safety standards or result in a significant reduction in costs for consumers. The MMA also requires the HHS Secretary to issue regulations that would grant waivers to individuals to import drugs for personal use under certain circumstances.Importation of prescription drugs under conditions set forth first by the MEDS Act, and kamagra oral jelly best price then by the MMA, could allow wholesalers and pharmacists to obtain FDA-approved drugs at lower prices than are available in the U.S. By purchasing them from foreign sellers, and pass these savings on to U.S.

Consumers.4. Why have prescription drug importation proposals not been implemented in the past?. Up until the Trump Administration’s final rule authorizing importation of prescription drugs from Canada, no previous HHS Secretaries have certified an implementation plan for importation, primarily due to safety concerns.

According to the HHS taskforce report on drug importation issued in December 2004, the drug distribution network for prescription drugs in the U.S. Is a “closed” system that provides the American public with multiple levels of protection against receiving unsafe or poor quality medications. Importation, according to the taskforce report, would create an opening in this closed system that would increase the opportunity for counterfeit, substandard, or unapproved products to enter the supply chain, introducing additional risks to American consumers.The report also noted some potential risks and challenges with legalizing importation, including but not limited to.

The increasing difficulty of monitoring and ensuring the safety of imported drugs. The additional cost and resources needed for ensuring safety, which may reduce potential savings. The possibility that total savings would be significantly less than international price comparisons suggest.

And the likelihood that there would be a reduction in research and development of new drugs. Furthermore, many former HHS Secretaries and FDA commissioners have voiced concerns in recent years about FDA’s ability to assure the safety, effectiveness, and quality of imported drugs. According to a 2017 letter to Congress signed by four former FDA commissioners:“…Allowing importation of drugs purported to be manufactured overseas in FDA-inspected facilities and drugs purported to be manufactured domestically for export to other countries and reimported from those countries to the United States cannot meet the requirements under the existing closed drug manufacturing and distribution system because the drugs could not be tracked and certified by the manufacturer…Such a program would be very different from importation of consumer products like watches or clothing, where consumers can more easily discern quality and where there are no health consequences of fake products.

It could lead to a host of unintended consequences and undesirable effects, including serious harm stemming from the use of adulterated, substandard, or counterfeit drugs. It could also undermine American confidence in what has proven to be a highly successful system for assuring drug safety.”5. What drug importation plans have been finalized?.

In September 2020, the Trump Administration issued a final rule and final FDA guidance for the importation of prescription drugs. The final rule would authorize states, territories and Indian tribes, and in certain future circumstances wholesalers and pharmacists, to implement time-limited importation programs, known as Section 804 Implementation Programs or SIPs, for importation of prescription drugs from Canada only. States, territories, and Indian tribes could submit proposals to the HHS Secretary to manage these SIPs and act as SIP sponsors.In order for a proposal to be approved by HHS, a SIP sponsor would need to specify.

The drugs it seeks to import. The foreign seller in Canada that would purchase the drug directly from its manufacturer. The importer in the U.S.

That would buy the drug directly from the foreign seller in Canada. The re-labeler or re-packager of the drug itself that would ensure the drug meets all labeling requirements in the U.S.. The qualifying lab that would conduct testing of the drug for authenticity and degradation.

And steps that would be taken by the SIP to ensure the supply chain is secure. SIPs would initially be authorized for 2-year periods with the possibility of 2-year extensions.Each SIP sponsor would also be subject to post-importation requirements, including providing FDA with data and information on the SIP’s cost savings to American consumers.The final FDA guidance specifies how manufacturers can import and market FDA-approved drugs in the U.S. That were manufactured abroad and intended to be marketed and authorized for sale in a foreign country.

Using this approach, a manufacturer may be able to obtain an additional National Drug Code (NDC) for drugs imported into the U.S. The stated rationale is that “in recent years, multiple manufacturers have stated (either publicly or in statements to the Administration) that they wanted to offer lower cost versions but could not readily do so because they were locked into contracts with other parties in the supply chain. This pathway would highlight an opportunity for manufacturers to use importation to offer lower-cost versions of their drugs.”6.

Which drugs would be covered under the new importation plans?. Under the final rule, which allows states and other entities to facilitate importation of drugs from Canada, only drugs that are currently marketed in the U.S. Would be eligible for importation.

As under current law, certain types of drugs are excluded from the definition of a prescription drug eligible for importation including. Controlled substances, biological products (including insulin), infused drugs, intravenously injected drugs, and inhaled drugs during surgery. Furthermore, drugs that are subject to risk evaluation and mitigation strategies (REMS), which are high-risk products with serious safety concerns, such as opioids, are not eligible for importation.Under the final FDA guidance, which allows manufacturers to import drugs to the U.S.

That were manufactured and intended for sale in other countries (not limited to Canada), prescription drugs, including biological products excluded under the final rule, could be imported and made available to patients. These drugs must also currently be marketed in the U.S. To be eligible.7.

What is the estimated savings for these importation plans?. The potential cost savings from the final rule are unknown. In the final rule itself, and in FDA’s full final regulatory impact analysis, the Trump Administration did not provide an estimate of the expected savings.

The final regulatory analysis noted that responses by other stakeholders, such as Canadian regulatory agencies and drug manufacturers, could impact the potential benefits of this program.The Trump Administration did not release an estimate of potential savings for importation in the FDA guidance for industry.8. What are states currently doing regarding importation?. Some states have been actively pursuing legislative action to promote the importation of prescription drugs.

Several states, including Florida, Vermont, Colorado, Maine, New Mexico, and New Hampshire have enacted laws establishing importation programs for prescription drugs from Canada. In order for any importation plan to go into effect, the HHS Secretary must certify that it meets the safety and cost saving requirements set forth in Section 804 of the FD&C Act. Under each state’s respective laws to establish an importation program, they are required to submit a proposal to HHS to demonstrate how its program will meet those safety and cost saving requirements.

Thus far, no state plan has been certified.Florida, Vermont, Colorado, and Maine have taken action to become the first states to implement importation plans. In August 2019, Florida officially submitted its importation proposal to HHS (predating the previous Administration’s rule for state importation plans). Under Florida’s importation plan, the program would be overseen by the state’s Agency for Health Care Administration (AHCA) through a vendor who would handle the operation of the program and ensure importers are following all state and federal laws relating to importation.

Eligible importers would be limited to wholesalers or pharmacists who dispense prescription drugs on behalf of public payers, including Medicaid, the Department of Corrections, and the Department for Children and Families. In June 2020, Florida’s AHCA released an “Invitation to Negotiate” for the state’s vendor bid system, for assistance with implementation of the importation program, and in December 2020, the AHCA contracted with a vendor to administer the importation program. The governor of Florida has called on the Biden Administration to approve the state’s plan, citing projections that it could “potentially save the state between $80 to $150 million in the first year alone.”Vermont submitted its importation proposal to HHS in November 2019.

Vermont’s plan primarily differs from Florida’s in that wholesalers would import drugs on behalf of both commercial plans and public payers, rather than just public payers.Colorado submitted its importation proposal in March 2020, and in January 2021, released an invitation to negotiate with vendors to implement its importation program. Bids were due in late April and the contract is set to be awarded later in 2021. New Mexico and Maine have also submitted importation plans for HHS approval.

New Hampshire is also in the process of developing importation plans for HHS approval, and according to the state’s law, New Hampshire had until February 1, 2021 to submit its plan. North Dakota passed a bill that requires a study on the potential impacts of prescription drug importation. Other states are also considering legislation that would facilitate drug importation from Canada, but thus far, none have been approved by HHS.9.

Under what circumstances can individuals legally import drugs from other countries, like Canada?. In most circumstances, it is illegal for individuals to import FDA-approved drugs from other countries for personal use. However, based on changes enacted by the MMA, personal importation of prescription drugs that have not been approved by the FDA for use in the U.S.

Is permitted on a case-by-case basis. Under this statutory authority, FDA has put out guidance that lays out certain circumstances where importation of non-FDA approved drugs for personal use might be allowed. For example, personal importation is generally allowed if the treatment is for a serious condition, there is no effective treatment available in the U.S., and there is no commercialization of the drug for U.S.

Residents. Typically, only a three-month supply is allowed, and individuals most confirm in writing that the drug is for personal use and provide information about the physician responsible for their treatment.There appears to be little enforcement by the FDA of the ban against importing FDA-approved drugs for personal use. Even if the personal importation of a drug is technically illegal, current law directs the FDA to exercise discretion in permitting personal importation of drugs when the product is “clearly for personal use, and does not appear to present an unreasonable risk to the user,” which is reinforced in FDA guidelines.The Trump Administration’s executive order from July 2020, which directed the HHS Secretary to finalize rulemaking in regard to states importing certain drugs from Canada, also directed HHS to take action to allow individuals to import prescription drugs from foreign countries as well as permit insulin products that were manufactured in the United States and sent abroad to be reimported to the United States.

In response, the previous Administration issued two requests for proposals, and HHS and FDA started accepting proposals for these two pathways in September 2020. However, the Biden Administration did not receive any proposals to be implemented via either of these pathways, and in June 2021, the Biden Administration formally withdrew both requests for proposals.10. How do stakeholders and the public view these importation plans?.

Many stakeholders have expressed reservations about the feasibility of the current importation plans. Prime Minister Trudeau stated that ensuring the safe and adequate supply of prescription drugs for Canadians is his first priority. However, he also said the Canadian government will take into account the actions of the United States and may be able to provide help to the US and other countries.

The Government of Canada stated that it would be unable to meet the needs of the U.S. Market without impacting access to medications for Canadians. The Canadian government also expressed concern that this policy would create drug shortages in Canada, and issued an order in November 2020 prohibiting the distribution of drugs that could cause or exacerbate a shortage.As mentioned above, industry groups such as PhRMA, as well as the Partnership for Safe Medicines and the Council for Affordable Health Coverage, sued the Trump Administration to keep the first importation plan under the final rule from going into effect, arguing that importation would weaken safeguards protecting America’s drug supply, expose Americans to substandard and counterfeit drugs, and that the additional resources required to ensure the safety of drugs from abroad would outweigh any potential savings for patients.

In addition to its lawsuit challenging the final rule, PhRMA has also filed citizens petitions challenging the state SIP applications submitted to HHS by Florida and New Mexico.Some organizations also submitted comments for the importation pathway described in the final FDA guidance. Despite their support for the flexibility to sell drugs under different NDC codes, PhRMA had specific concerns with guidance, including that NDC flexibility alone is not enough to lower prices for consumers. The American Medical Association (AMA) and APhA also expressed concern with the FDA guidance, noting the potential for unintended consequences, including increased costs for patients and patient and pharmacy confusion, leading to disruptions in patient care.Other stakeholders, however, have expressed support for allowing prescription drug importation, including AARP, the AMA, National Federation of Independent Business (NFIB), and Patients for Affordable Drugs Now, although some of these groups expressed concerns about specific aspects of the importation plan at the proposed rule stage.

Patients for Affordable Drugs Now said it was pleased the Administration had opened the door for importation, but noted that it is not a solution for lowering drug prices for the majority of Americans.The American public is generally in favor of importation. According to KFF polling from October 2019, 78% of the public favors allowing Americans to buy prescription drugs imported from licensed Canadian pharmacies. This proposal has broad support across party lines – 75% of Democrats, 82% of Independents, and 75% of Republicans favor drug importation from Canada (Figure 1).

However, it not clear to what extent public opinion would shift if presented with arguments for or against importation.The American public also supports virtually all proposals to lower prescription drug costs, including the government negotiating with drug companies, and believes lowering prescription drug prices should be a top legislative priority for Congress..

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Kim Vitelli es la administradora de la Oficina de Inversión en la Fuerza Laboral del Departamento de Trabajo de EE.UU.Cristina Barillas met Deputy Secretary of Labor Julie Su in October at an event for Latina Equal Pay Day – the day that marks how many months into the year it takes Latinas to earn the same amount as their non-Hispanic white male counterparts in the year before. We asked Cristina to share her experience as a woman who worked her way into a profession traditionally segregated by race and gender, and what that good job means to her and her family. Tell us about yourself. How did you choose this field of work?. I always find this funny when asked.

I believe plumbing choose me, not me it. It was at a point in my life when I needed a job that was more stable, and at that same time a friend suggested I try getting into the trades. In 1998 I applied to both the Electricians Local 134 IBEW and Plumbers Local 130 UA. In January of 2000, I had just reapplied for the electricians and was about to reapply to the plumbers, when I received my acceptance letter to Local 130. What is your favorite part of the job?.

This has changed over the years. I am thrilled to build something, fix something or even diagnose a problem, but it’s not just the work. What I love more is the sisterhood and brotherhood of helping my fellow plumbers succeed. That is what my motto is. €œI am here to make your journey better than mine.” What resources – job trainings, career development, etc.

€“ did you use?. I wasn’t introduced to Chicago Women in Trades (CWIT) until 2003 and since then I have always participated as much as I can. When people ask me for assistance in getting their daughter, sister or friend into plumbing, I always suggest going through CWIT Technical Opportunities Program (TOP). There is nothing like CWIT TOP. You can learn about every trade, and not only by reading or meeting a person in a trade, but hands on.

A woman can determine what trade would best suit her, and then start creating her own sister group with the other ladies in the program. CWIT is a vital organization. Besides TOP, it is a safe space for women to continue learning their trade with other sisters and a space with no fear of judgement, rejection or harassment. I have heard many sisters call CWIT “home.” We also formed Women of 130, a group specifically for Local 130 women (apprentices, journeymen or retirees). We saw a need to ensure that women could complete the program and remain in the local to finish out their career.

We have seen many sisters fall victim to the ebbs and flows of our trade, so we created an environment where our sisters felt encouraged, supported and accepted. What would you say to a woman who wants to join your industry but is hesitant?. I would tell her to get in touch with CWIT or any similar organization. If you want to start in a trade or you’re curious about the trade, this is where you start. CWIT will introduce you to the trades, they will help fill out the applications, they will help you study (for both the written and physical exam), and they will encourage you.

Plus, it’s a great way to meet women that are in the trades, doing what one day you could possibly be doing. As far as plumbing, I would tell her, “I love my trade, my sisters, my brothers, there is nothing like the fulfillment of plumbing, 'we protect the health of the nation.'” Editor's note. Chicago Women in Trades is also a WANTO grantee. Learn more about the U.S. Department of Labor's Women in Apprenticeship and Non-Traditional Occupations grant program..

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We can also help you assess costs and find financial aid. For job hunters, we’ve got tips on resumes, networking and interviews. You can find all of these resources online, or by contacting one of the 2,320 American Job Centers around the country to learn more about their services and arrange a visit. Earn while you learn If you want to gain new skills while pulling in a paycheck, you should definitely consider an apprenticeship. You can get paid while gaining the skills, experience and credentials that employers want.

The average annual starting salary of apprenticeship grads is $72,000, and apprenticeships are available in a wide and growing variety of occupations. Sound interesting?. Learn more at apprenticeship.gov. Find a new field Maybe you’re happy with the skills you’ve got, but you’re still looking for a change. With MyNextMove.org, you can search careers by key words, browse by industry, or answer questions about the type of work you’d like to do and we’ll show you relevant job options.

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Careers begin here Job Corps offers free training and education for people ages 16-24, and is now accepting enrollment for in-person instruction. Explore and compare career paths in dozens of in-demand fields at jobcorps.gov/train. Get the details Let’s say you’ve narrowed down your options and you’re starting to wonder which one offers the best opportunities. The Bureau of Labor Statistics’ Occupational Outlook Handbook is your next stop. Select the occupational field you’re considering, and the handbook will provide tons of information, including.

Educational requirements Median annual salary Projected growth You can also browse occupations by pay, speed and size of growth and educational requirements. People are looking for work all over America. Help us connect them with good jobs by sharing this information with them!. Kim Vitelli is the administrator of the Office of Workforce Investment at the U.S. Department of Labor.

¿Busca Trabajo?. Nosotros le Podemos Ayudar Por Kim Vitelli Últimamente hemos visto mucho movimiento en el mercado laboral. En agosto hubo 10,4 millones de vacantes disponibles, se hicieron 6,3 millones de contrataciones y se registraron 4,3 millones renuncias. La tasa de abandonos aumentó en un 2.9%, el porcentaje más alto desde que comenzamos a rastrear datos. En otras palabras, hay muchos trabajos disponibles y muchas personas buscando algo nuevo.

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Gane mientras aprende Si desea adquirir nuevas habilidades al mismo tiempo que recibe un cheque de pago, definitivamente debería considerar un aprendizaje. Se le puede pagar mientras adquiere conocimientos, experiencia y credenciales que quieren los empleadores. El salario inicial promedio anual de los graduados de aprendizaje es de $72,000, y hay aprendizajes disponibles en una amplia http://www.ec-rodolphe-reuss-ii-strasbourg.ac-strasbourg.fr/wp/?p=2461 y creciente variedad de ocupaciones. ¿Suena interesante?. Sepa más en apprenticeship.gov.

Encuentre un nuevo campo Tal vez esté satisfecho con las habilidades que tiene, pero aún está buscando un cambio. Con MyNextMove.org puede buscar carreras por palabras clave, navegar por sectores o responder preguntas sobre el tipo de trabajo que le gustaría hacer y le mostraremos opciones de trabajo relevantes a esa búsqueda. Cada página incluye los conocimientos, habilidades y destrezas clave que necesitará. Existe una versión de esta herramienta en español (Mi Próximo Paso) y otra sólo para veteranos (My Next Move for Veterans) que ajusta los códigos de clasificación militar con las carreras civiles. MySkillsMyFuture puede ayudarlo a encontrar y explorar nuevas trayectorias laborales.

Simplemente ingrese su trabajo actual o pasado, y le proporcionaremos una lista de empleos junto con las habilidades necesarias. Haga clic en cualquiera que parezca interesante y aprenda más sobre ellos. Las carreras comienzan aquí Job Corps ofrece capacitación y educación gratuitas para personas de entre 16 a 24 años, y ahora acepta inscripciones para instrucción en persona. Explore y compare trayectorias ocupacionales en docenas de campos demandados en jobcorps.gov/train. Obtenga los detalles Supongamos que ya ha concretado sus opciones y está empezando a preguntarse cuál ofrece las mejores oportunidades.

El Manual de Perspectivas Ocupacionales de la Oficina de Estadísticas Laborales es su próxima parada. Seleccione el campo ocupacional que está considerando y el manual proporcionará muchísima información, incluyendo. Requisitos educativos Salario medio anual Proyección de crecimiento También puede buscar ocupaciones por salario, ritmo y tamaño del crecimiento, y requisitos educativos. La gente está buscando trabajo por todo Estados Unidos. ¡Ayúdenos a conectarlos con buenos trabajos compartiendo esta información con ellos!.

Kim Vitelli es la administradora de la Oficina de Inversión en la Fuerza Laboral del Departamento de Trabajo de EE.UU.Cristina Barillas met Deputy Secretary of Labor Julie Su in October at an event for Latina Equal Pay Day – the day that marks how many months into the year it takes Latinas to earn the same amount as their non-Hispanic white male counterparts in the year before. We asked Cristina to share her experience as a woman who worked her way into a profession traditionally segregated by race and gender, and what that good job means to her and her family. Tell us about yourself. How did you choose this field of work?. I always find this funny when asked.

I believe plumbing choose me, not me it. It was at a point in my life when I needed a job that was more stable, and at that same time a friend suggested I try getting into the trades. In 1998 I applied to both the Electricians Local 134 IBEW and Plumbers Local 130 UA. In January of 2000, I had just reapplied for the electricians and was about to reapply to the plumbers, when I received my acceptance letter to Local 130. What is your favorite part of the job?.

This has changed over the years. I am thrilled to build something, fix something or even diagnose a problem, but it’s not just the work. What I love more is the sisterhood and brotherhood of helping my fellow plumbers succeed. That is what my motto is. €œI am here to make your journey better than mine.” What resources – job trainings, career development, etc.

€“ did you use?. I wasn’t introduced to Chicago Women in Trades (CWIT) until 2003 and since then I have always participated as much as I can. When people ask me for assistance in getting their daughter, sister or friend into plumbing, I always suggest going through CWIT Technical Opportunities Program (TOP). There is nothing like CWIT TOP. You can learn about every trade, and not only by reading or meeting a person in a trade, but hands on.

A woman can determine what trade would best suit her, and then start creating her own sister group with the other ladies in the program. CWIT is a vital organization. Besides TOP, it is a safe space for women to continue learning their trade with other sisters and a space with no fear of judgement, rejection or harassment. I have heard many sisters call CWIT “home.” We also formed Women of 130, a group specifically for Local 130 women (apprentices, journeymen or retirees). We saw a need to ensure that women could complete the program and remain in the local to finish out their career.

We have seen many sisters fall victim to the ebbs and flows of our trade, so we created an environment where our sisters felt encouraged, supported and accepted. What would you say to a woman who wants to join your industry but is hesitant?. I would tell her to get in touch with CWIT or any similar organization. If you want to start in a trade or you’re curious about the trade, this is where you start. CWIT will introduce you to the trades, they will help fill out the applications, they will help you study (for both the written and physical exam), and they will encourage you.

Plus, it’s a great way to meet women that are in the trades, doing what one day you could possibly be doing. As far as plumbing, I would tell her, “I love my trade, my sisters, my brothers, there is nothing like the fulfillment of plumbing, 'we protect the health of the nation.'” Editor's note. Chicago Women in Trades is also a WANTO grantee. Learn more about the U.S. Department of Labor's Women in Apprenticeship and Non-Traditional Occupations grant program..

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