Anne Swearingen, DBA, MSN

Adjunct Professor at St. Cloud State University
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Contact Information
us****@****om
(386) 825-5501
Location
Greater Minneapolis-St. Paul Area
Languages
  • English Native or bilingual proficiency
  • French Limited working proficiency

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Credentials

  • Team Coach Certification Program
    LIM: Leadership in Motion.
    Aug, 2023
    - Oct, 2024
  • Sustainability Mindset
    Principles for Responsible Management Education (PRME)
    Dec, 2022
    - Oct, 2024
  • Sustainability Mindset Action Lab
    Principles for Responsible Management Education (PRME)
    Oct, 2022
    - Oct, 2024

Experience

    • United States
    • Higher Education
    • 700 & Above Employee
    • Adjunct Professor
      • Sep 2017 - Present

      Adjunct Professor in School of Science and Engineering, Master of Applied Clinical Research. • Developed and implemented course syllabi, lesson plans, and assessments. • Facilitated active learning through class discussions, groups activities, and individual projects. • Provided constructive feedback on student assignments to promote student success. • Evaluated student performance using appropriate assessment techniques and provided timely feedback. • Mentored students in the development of their research skills and critical thinking abilities. Show less

    • United Kingdom
    • Medical Equipment Manufacturing
    • 700 & Above Employee
    • Director of Medical Operations & Effectiveness
      • Mar 2021 - Apr 2023

      Responsible for strategic Global Operational tasks within the Medical and Clinical Team. • Implemented strategic programs to improve efficiency and ensure compliance with local and global regulations. • Monitored legislative changes that could affect the organization’s operations. • Cultivated and maintained positive working relationships with employees, executives, and other stakeholders. • Built talent pipeline to support business growth and enduring success. • Researched underlying issues, regulatory compliance status and processes to resolve complex business issues and recommended strategic corrective actions. • Negotiated contracts with vendors. • Managed and oversaw leadership team to meet established KPIs and achieve objectives and key results. • Maintained effective communication channels with all stakeholders involved in the organization’s activities. Show less

    • Director, Global Operations - Medical and Clinical Affairs
      • Jan 2019 - Mar 2021

      Ensuring successful management and execution of Compliance and Operation activities within the Health Care Compliance and Clinical Research Organization.• Collaborated with senior leadership to set strong long-term objectives for the organization.• Managed budgeting and financial planning for the organization.• Directed the organization’s daily operations, ensuring compliance with applicable laws and regulations.• Created detailed plans outlining timelines, goals, budgets, staffing needs and other requirements for projects.• Monitored market conditions and competitor activities to inform business decisions. • Developed and implemented comprehensive strategies to improve operational processes and organizational efficiency. Show less

    • Manager Clinical Operations
      • Aug 2017 - Jan 2019

      Responsible for management of clinical team for Critical and Chronic Care Solutions.• Partnered with portfolio leaders to assess and prioritize clinical research.• Developed and implemented clinical operations processes, ensuring compliance with regulations and laws.• Coordinated the development of clinical protocols, informed consent forms, case report forms and other study documents.• Managed the recruitment process for clinical research sites.• Collaborated closely with internal teams such as Regulatory Affairs, Quality Assurance and Other stakeholder to ensure successful execution of research projects. Show less

    • United States
    • Medical Equipment Manufacturing
    • 700 & Above Employee
    • Sr. Manager, Clinical Operations - Safety
      • Aug 2013 - Aug 2017

      Responsible for managing the safety trial operations team within clinical operations. Adherence to global regulatory requirements for adverse event and device deficiency reporting. Management of Clinical Events Committees. Responsible for the selection, development and retention of team members.

    • Sr. Clinical Program Manager
      • Jul 2011 - Aug 2013

      Responsible for driving the strategy and managing the execution of global clinical programs worldwide through clinical project managers and involving departmental and cross-functional teams in support of the organizations business objectives for product development and/or commercialization.Leading, directing and executing clinical programs worldwide in accordance with strategy, project plans, approved budget and resource allocations while following applicable regulatory and standard operating procedures.Recruitment, management and development of direct reports. Mentoring and coaching all levels of Project Management.Leading and driving the project team in the planning, execution and management of all operational aspects of clinical trials and proactive identification, assessment, and management of clinical study risks. Show less

    • Manager, Clinical Programs CRV
      • Sep 2008 - Jun 2011

      Responsible for driving the strategy and managing the execution of Canadian clinical programs for mutilate therapeutic areas and involving departmental and cross-functional teams in support of the organizations business objectives for product development and/or commercialization.Leading, directing and executing Canadian clinical programs in accordance with strategy, project plans, approved budget and resource allocations following applicable regulatory and standard operating procedures.CRM Director's Award, 2009, for clinical contribution to the Canadian organization.Demonstrated commitment to patient safety and product quality by maintaining compliance to the Quality Policy and other documented quality processes and procedures. Show less

    • United States
    • Medical Device
    • 100 - 200 Employee
    • Clinical Affairs Manager
      • Jan 2008 - Aug 2008

      Managed and coordinated clinical studies for all business units in the United States and Belgium. Communicated directly with internal and external stakeholders. Designed a clinical strategy for revising and improving standard operating procedures for US based and International clinical studies, in order to improve quality and efficiency. Collaborated with other functional areas in new product development, providing guidance regarding the quality and type of clinical study necessary to support a new product to market. Preparation of reports for submission to regulatory agencies. Show less

    • United States
    • Medical Equipment Manufacturing
    • 700 & Above Employee
    • Field ClinicalEngineer
      • Oct 2002 - Jan 2008

      Responsible for technical expertise of medical devices. Clinical Site management of all aspects of clinical trials Responsible for technical expertise of medical devices. Clinical Site management of all aspects of clinical trials

    • Research Coordinator
      • May 2000 - Oct 2002

      Managed clinical trials at the office level Managed clinical trials at the office level

Education

  • Saint Mary's University of Minnesota
    Doctorate of Business Administration
    2019 - 2023
  • Union University
    Master of Business Administration (MBA)
    2005 - 2007
  • The University of Tennessee Health Science Center
    MSN
    2001 - 2002
  • University of Windsor
    BScN
    1996 - 1998
  • Nicholson Catholic College
    Dip.
    1986 - 1991

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