Auditing Director jobs in Massachusetts

Auditing Director executes a comprehensive enterprise-wide internal auditing strategy, function, and practice adhering to auditing standards and regulatory requirements. Uses auditing governance frameworks and procedures to plan and manage the auditing schedules, projects, teams, and tasks required to meet defined objectives. Being an Auditing Director engages with other functions across the enterprise, like risk, finance, information technology, and security, to facilitate audits. Prepares audit reports and recommends enhanced controls or processes as needed. Additionally, Auditing Director builds auditing teams and expertise with coaching and developmental initiatives. Requires a bachelor's degree. Typically requires a Certified Public Accountant (CPA). May sometimes require Certified Internal Auditor (CIA). Typically reports to a director. The Auditing Director typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. To be an Auditing Director typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. (Copyright 2024 Salary.com)

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Senior Global Development Scientist Director
  • 10001087 - Director Clinical Research
  • Boston, MA FULL_TIME
  • Job Title: Senior Global Development Scientist Director

    Locations: In Office in one of these locations - Boston Seaport, Warsaw PO, Barcelona SP or Mississauga CA

    As a Senior Global Development Scientist Director (SGDSD) you will independently provide scientific and clinical input to all aspects of late stage product development. This includes but is not limited to the design, delivery and interpretation of pivotal clinical trials and of studies that further characterize the overall benefit and risk and value of Respiratory and Immunology products in late stage development. This role ensures that the safety evaluation process for the pivotal phase III trials is seamless and complete.

    In this role you will seek input from the appropriate functional experts and will coordinate these activities in support of clinical studies and programs.

    The SGDSD works as a member of a diverse and motivated team of researchers spanning across multiple divisions of Biopharmaceutical Units. The objectives of this role are set by the Global Clinical Program Lead in agreement with Global Clinical Head(s). The role will have a special focus on late stage clinical trials within respiratory & immunology where this role will work in close collaboration with the study team physician with all aspects of scientific input, clinical data quality metrics and safety evaluation.

    The Senior Global Development Scientist Director independently leads many activities and contributes to science stories, regulatory submissions, process improvement and mentoring scientists and physicians.

    Typical Accountabilities

    • Providing scientific leadership in the innovative design, execution and interpretation of clinical trials in one or more development programs.
    • Expected to effectively collaborate with colleagues in other functions including Patient Safety, Regulatory Affairs, Clinical Operations, and Early Development groups.
    • Be involved primarily in Late Phase (Ph2b and Phase 3) clinical programs but will collaborate with clinical colleagues supporting Early Phase programs as well as Medical Affairs colleagues.
    • Provide expert scientific data/analysis into the preparation of regulatory documents and interactions with regulatory authorities.
    • Provide expert scientific analysis and interpretation of data from ongoing studies and from within the literature.
    • Lead development of quality metrics and data review plan for assigned studies.
    • Support and contribute to Medical Monitoring of trials.
    • Lead and participate in activities that ensure quality, consistency and integration of clinical study related results and ensure a robust safety evaluation process within the clinical team.
    • Provide scientific evidence to support strategic decision making for R&D, marketing, clinical, and business development departments.
    • Participate in the preparation of scientific publications and present scientific results and study protocol to multidisciplinary teams and key partners.
    • Develop and review different clinical documents such as protocols, informed consent, investigator’s brochure, study report, briefing books.
    • Provide scientific input to TA standards

    Education, Skills and Experience Required

    • Scientific doctoral level degree (e.g. PhD or PharmD), relevant clinical qualification, or other relevant university degree with extensive experience from Late Phase clinical development within the industry.
    • Ten or more years of relevant pharmaceutical industry experience (multi-country clinical trials).
    • Understanding of scientific and clinical issues related to the design and implementation of clinical trials and interpreting trial results.
    • Demonstrated ability to work collaboratively in a cross-functional setting, particularly with patient safety, vendors, CRAs, site staff and clinical operations.
    • Experience with regulatory submissions, LCM, advisory boards, annual safety updates.
    • Experience with dermatology and/or rheumatologic therapeutic areas preferred.

    Employer of Choice:

    At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and ignite your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society.

    AstraZeneca is committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be! We encourage and consider applications to join our team from all qualified candidates, regardless of their characteristics.

    We offer a competitive Total Reward program including a market driven base salary, bonus and long term incentive. We also provide a generous paid time off program and a strong benefits array of offerings.

    When we put unexpected teams in the same room, we spark bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our outstanding and high-reaching world.

    AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

    AstraZeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.

  • 4 Days Ago

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Global Development Medical Director - Diabetes/Obesity/MASH
  • 50056669 - Assoc Director Physician
  • Boston, MA FULL_TIME
  • At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality! If y...
  • 21 Days Ago

1
Senior Medical Director, Late Clinical Development – Diabetes/Obesity
  • 10001001 - Director Physician
  • Boston, MA FULL_TIME
  • Senior Medical Director, Late Clinical Development – Diabetes/Obesity Do you have expertise in Clinical Research and Development combined with a deep understanding of the medical aspects of drug devel...
  • 5 Days Ago

1
Senior Medical Director, Metabolism/Obesity, Early Clinical Development, CVRM
  • 10001001 - Director Physician
  • Boston, MA FULL_TIME
  • Senior Medical Director, Metabolism/Obesity, Early Clinical Development, CVRMAre you an experienced endocrinologist/obesity specialist with clinical expertise in the management of patients with metabo...
  • 12 Days Ago

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QA Auditing Specialist
  • IWP
  • Andover, MA FULL_TIME
  • The Auditing Specialist will work as a member of the QA team, under the direction of the Senior Manager of Business Process, Projects and Quality, to develop, implement and maintain QA plans that alig...
  • 1 Month Ago

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FME Auditing and Accounting Mentor
  • Babson College
  • Wellesley, MA PART_TIME
  • About Us We’re all different. We’re all Babson. Babson College is a world-class business school, empowering entrepreneurial leaders to create great economic and social value - everywhere. Here you’ll ...
  • 27 Days Ago

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Audit Director - Operations
  • U.S. Bancorp
  • New York, NY
  • The Corporate Audit Services Audit Director supports the Senior Audit Director and Chief Audit Executive, in providing t...
  • 3/27/2024 12:00:00 AM

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Audit Director / Audit Evaluator Director - Delivery & Retail Operations Directorate
  • Usps Oig
  • **Audit Director / Audit Evaluator Director - Delivery & Retail Operations Directorate** Location: Arlington, Virginia; ...
  • 3/27/2024 12:00:00 AM

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SEC Audit Director
  • Kunin Associates
  • Miami, FL
  • Job Description Job Description South Florida established CPA firm is seeking an Audit Director/Partner with SEC experie...
  • 3/26/2024 12:00:00 AM

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Audit Director- CPA
  • Marcum Search
  • New York, NY
  • Job Description Job Description Marcum Search LLC is recruiting for a Senior Audit Manager or Audit Director, (depending...
  • 3/25/2024 12:00:00 AM

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Audit Director
  • Nesco Resource
  • Bohemia, NY
  • AUDIT DIRECTOR/HYBRID/$150k - $170k Embark on an exhilarating journey as the Internal Audit Director at one of Long Isla...
  • 3/25/2024 12:00:00 AM

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Business Assurance (Audit) Director (Real Estate)
  • Moore Colson
  • Atlanta, GA
  • Moore Colson is a premier, full-service certified public accounting (CPA) and consulting firm in Atlanta with over 40 ye...
  • 3/25/2024 12:00:00 AM

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Director
  • Chick-fil-A
  • Clinton, MD
  • Chick-fil-A Woodyard Landing in Clinton, MD is looking for a passionate and experienced Director to lead a seasoned and ...
  • 3/25/2024 12:00:00 AM

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Internal Audit Director
  • Spartan Placements LLC
  • Bohemia, NY
  • Internal Audit Director We anticipate the Internal Audit Director will perform the following responsibilities: Client Se...
  • 3/24/2024 12:00:00 AM

Massachusetts is the 7th-smallest state in the United States. It is located in the New England region of the northeastern United States and has an area of 10,555 square miles (27,340 km2), 25.7% of which is water. Several large bays distinctly shape its coast. Boston is the largest city, at the inmost point of Massachusetts Bay, and the mouth of the Charles River. Despite its small size, Massachusetts features numerous topographically distinctive regions. The large coastal plain of the Atlantic Ocean in the eastern section of the state contains Greater Boston, along with most of the state's po...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Auditing Director jobs
$194,263 to $259,399

Auditing Director in Richmond, VA
The “human touch” of audit stems from the basic concept of treating those who you are auditing as you would want to be treated if you were the one being audited.
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Boards of Directors and their committees rely on management to run the daily operations of the business.
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Auditing Director in Cedar Rapids, IA
As part of the audit team, the Director will be responsible for.
December 29, 2019