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Amy Hurst

Clinical Research Coordinator at University of Michigan

Professional Background

Amy Hurst is a dedicated and highly skilled clinical subject coordinator, bringing over 15 years of invaluable experience in the realm of pre-clinical and clinical trials. Throughout her impressive career, Amy has showcased a profound ability to manage and coordinate the intricacies of multiple clinical research trials simultaneously. Her expertise lies in her adeptness at liaising effectively with a variety of stakeholders, including doctors, departments, and pharmaceutical companies, to ensure seamless communication and collaboration among project teams.

In her role, Amy has not only excelled at coordination but has also cultivated a strong skill set in the technical aspects of clinical research. She is well-versed in writing research protocols, navigating Institutional Review Board (IRB) submissions, and utilizing REDCap databases and coding systems. This combination of administrative and technical skills allows Amy to carry out research projects efficiently while adhering to strict compliance measures.

Amy’s proactive nature drives her to continuously seek and implement improvements within her work settings. Her efforts focus on enhancing operational efficiency and achieving cost savings, making her a valued asset in any clinical research environment.

Education and Achievements

Amy Hurst obtained her Bachelor of Science (BS) degree from the esteemed University of Michigan, where she cultivated a strong foundation in scientific principles, critical thinking, and research methodology. Additionally, she earned an Associate of Science (A.S.) degree from Kalamazoo Valley Community College, which further enhanced her academic background and equipped her with essential skills for her career in clinical research.

Throughout her educational journey and professional experience, Amy has been associated with some of the leading medical and research institutions, particularly the University of Michigan. Her extensive involvement in various capacities demonstrates her commitment to advancing medical research and contributing to the betterment of healthcare.

Previous Roles

Amy has held several key positions within the University of Michigan’s clinical research landscape, including:

  • Clinical Research Coordinator at University of Michigan: Here, Amy coordinated complex clinical trials, working closely with medical teams and participants to facilitate successful outcomes.
  • Children's Clinical Subjects Coordinator at Michigan Medicine: In this role, she was responsible for coordinating research activities specifically involving pediatric subjects, ensuring that protocols were followed and that the unique needs of children participating in trials were met.
  • Research Laboratory Technician Senior at University of Michigan: As a senior technician, she applied her knowledge in laboratory settings, supporting ongoing research through data collection, analysis, and management.
  • Research Assistant at University of Michigan: In her earlier roles at the university, including her time as a research lab technician and laboratory assistant, Amy developed a robust understanding of laboratory processes and research methodologies.

Her educational and professional background has not only equipped her with the technical skills required for clinical research but has also fostered a strong sense of dedication towards improving patient outcomes, making her a respected professional in her field.

Notable Achievements

Amy Hurst is recognized for her impactful contributions to the field of clinical research. Her ability to streamline processes and enhance collaboration among diverse teams has led to successful clinical trials that provide vital data for advancing medical knowledge and patient care.

Moreover, her experience in preparing IRB submissions and crafting detailed research protocols has consistently resulted in smooth approvals, enabling projects to progress without significant delays. These skills reflect her comprehensive understanding of regulatory requirements and ethical considerations in clinical research.

Through her commitment to improving operational efficiency, Amy has also been instrumental in implementing cost-saving measures. By identifying areas for improvement and promoting best practices, she has contributed to more sustainable research processes that maximize resources while maintaining high-quality outcomes.

In summary, Amy Hurst stands out as a clinical subject coordinator whose career is marked by a balance of technical expertise and a passion for improving clinical outcomes. Her extensive background in clinical trials, coupled with her strong educational foundation, positions her as a leader in her field. Amy continues to inspire colleagues and contribute significantly to the advancing domain of clinical research.

Related Questions

How did Amy Hurst develop her expertise in managing multiple clinical research trials simultaneously?
What strategies has Amy Hurst implemented to improve efficiency and cost savings in clinical research?
In what ways has Amy Hurst contributed to the development and adherence of research protocols in her career?
How does Amy Hurst successfully liaise with various departments and pharmaceutical companies in her role?
What motivated Amy Hurst to pursue a career in clinical research after her education at the University of Michigan?
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Location

Ann Arbor, Michigan