director of tax salaries in boston, massachusetts

job summary: Our Boston based client is seeking a Senior Tax Accountant to join their team. This person will work closely with the International Tax team and have exposure to executive leadership. There is remote flexibility with as needed in-office time in downtown Boston.   location: Boston, Massachusetts job type: Permanent salary: $110,000 - 125,000 per year work hours: 9 to 5 education: Bachelor's degree experience: 5 Years   responsibilities: Work closely with the Tax team to complete the income tax compliance work for their international operations including completing 5471, 8858, 8865, and 1118 forms Help with GILTI, FDII, and BEAT calculationsReviewing US International tax provision on a quarterly basisOther duties as assigned  qualifications: Bachelor's degree in Accounting or equivalent CPA or M.S. in Taxation preferred 5+ years in public accounting and/or a corporate taxHigh proficiency with spreadsheets, databases, and tax applicationsStrong analytical skills and attention to detail Please click to apply and send qualified resumes to christina.pescia@tatum-us.com.   skills: Corporate Tax For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

job summary: We have partnered with a premiere financial institution in Boston with an opening for a Tax Manager. The Tax manager position is a great opportunity to work in a well established, growing company with an excellent reputation. This highly visibly Tax role offers an excellent culture, benefits and Work Life Balance.   location: Boston, Massachusetts job type: Permanent salary: $100,000 - 120,000 per year work hours: 9 to 5 education: Bachelor's degree experience: 7 Years   responsibilities: The Tax Manager duties include: Prepare and review tax provisions for partnership & Regulated Investment Company productsPrepare and review calculations for the year-end taxable income projections and distribution processConduct systems testing and contribute to system initiatives for new accounting and tax systemsResearch and analyze various tax- related calculations for REITs, partnerships and other investment types for tax reporting purposesProactively look for ways to improve processes and maximize efficienciesReview financial data to ensure accuracy for financials and disclosuresHire, train and motivate staffResearch and understand new pronouncements and report impact on funds as well as ensure compliance   qualifications: The ideal profile includes: BS in Accounting or Finance7 or more years of relevant tax experience including partnership Great communications skillsPrior management experience requiredAbility to manage multiple projects and deadlinesEnjoys leading and developing staff  skills: $1 - 2 billion For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilize Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Cambridge, Massachusetts job type: Contract salary: $150 - 165 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. Responsible for the development, maintenance, and implementation of Company Core Data Sheets (CCDS) in line with international standards and guidelines. Provide strategic and tactical labeling expertise to teams while ensuring compliance with applicable regulatory requirements.Serve as the regulatory expert for labeling on the global Regulatory Affairs (RA) Subteam to ensure that regulatory labeling requirements are met for assigned products.Leads cross functional teams to develop and update CCDS and other key global labeling documents (i.e. CCDS Working Team)In coordination with Global Labeling Oversight Committee (GLOC) Chair, manages review and approval of CCDS/resolution of labeling issues with the relevant GLOCEvaluates risks associated with CCDS content and implementation strategies, develops mitigation plans, and appropriately escalates issues to Global Labeling management and the Global Regulatory LeadRecommends strategies and labeling language for inclusion in key product labels (US PI, EU SmPC, JPI, others as appropriate), consistent with the overall product strategy and information in the CCDS, when available.Provides information to Global Labeling Compliance, as required, to support internal and external (i.e. Regulatory Authority) requirements and support audits/inspections as a labeling subject matter expertLiaises with US Labeling Operations and EU Labeling Operations to ensure labeling objectives and timelines are metAnalyzes relevant competitor labeling to ensure Takeda products have the most competitive labeling possible; maintain awareness of recent in-class approvals.Remains current with global standards, initiatives by regulatory authorities related to the CCDS and labeling, and assures that Takeda processes conform to regulatory requirements. Propose actions as needed.Prepares/leads training and information sessions with GRA and other functional areas to increase understanding and compliance with internal and external labeling expectations and optimal labeling strategies.Establishes and manages cross-functional relationships to ensure control and continuous improvement of global labeling programs to meet business needs and regulatory requirements.  qualifications: BSc Degree, preferred. BA accepted. Advanced scientific degree (MSc, PhD, or PharmD) preferred;8+ years of pharmaceutical industry experience. This is inclusive of 6 years of labeling experience or combination of 5+ years regulatory and/or related experience. Understanding of scientific principles and regulatory/quality systems relevant to drug development. Knowledge of global standards and regulations related to CCDS and Product Labeling (US PI and EU SmPC experience required, other regional labels also preferred). Strong oral and written communications, managing and adhering to timelines, negotiation skills, integrity and adaptability.Demonstrates problem-solving ability with ability to analyze risk and make appropriate recommendations/decisions. Must work well with others and within global teams. Acceptable and independent skills in the area of regulatory affairs such as understanding broad concepts within labeling and implications across the organization and globally; proactively identifies issues; offers creative solutions and strategies, including risk mitigation strategies.Responsible for demonstrating company leadership behaviors.Manual dexterity required to operate office equipment (i.e. computers, phones, etc.).Carrying, handling and reaching for objectsAbility to sit or stand for long periods of time while traveling.Willingness to travel to various meetings, including overnight trips. Requires approximately up to 10-30% travel.   skills: CMC, FDA, GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs Strategy, Submissions, ICH Regulations For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.