University of Alabama at Birmingham
September 22, 2023
Offerd Salary:$60,835 - $98,855
Working address:N/A
Contract Type:Other
Working Time:Negotigation
Working type:N/A
Ref info:N/A



Position Summary

This position will be responsible for managing and coordinating all aspects of assigned research studies within the UAB Alzheimer's Research Center. This position will develop protocol-specific systems and documents to ensure accuracy and completeness of research visits and documentation. This position will also be responsible for maintaining compliance with IRB for the assigned studies. All study activities will be conducted in accordance with the protocol, IRB regulations, and Good Clinical Practice (GCP). The mission of the UAB Alzheimer's Disease Center is to overcome Alzheimer's disease and related disorders by conducting, fostering, and enabling research at UAB and through national collaborations, by providing the highest level of care to patients and families, and by educating both professionals and the public about aging, dementia, and brain health. Our research is aimed at reducing Deep South disparities in Alzheimer's disease.

General Responsibilities

  • To manage all aspects of assigned clinical studies including education.
  • To develop protocol-specific systems and documents.
  • To act as a consultant within area of clinical expertise.
  • To identify various stakeholders to ensure adequate design, implementation, and testing of study aims.
  • To assess and determine solutions for operational shortcomings for data procurement in protocol design.
  • To maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations.
  • Primary Responsibilities

  • Develops protocol-specific systems and documents including process flows, training manuals, SOPs, and CRFs.
  • Assists with study budgets as needed.
  • Assists in maintaining compliance with federal, state, and accrediting agencies (sponsors), including maintaining any required documentation.
  • Prepares and submits multiple levels of research documentation (i.e. IRB, IND, or FDA submissions, educational materials, reports, grant renewal reports, and study forms).
  • Collects information to determine study feasibility.
  • Makes recommendations to investigators and oversight organizations, as appropriate.
  • Prepares for and leads team meetings for assigned studies.
  • Assists colleagues in identifying efficiencies and improving processes.
  • Perform other duties as assigned.
  • Annual Salary Range - $60,835 - $98,855



    Bachelor's degree in a related field and five (5) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred.

    Preferred Qualifications

    The ideal candidate will have previous research experience with exceptional customer service skills. A degree in Psychology is preferred, but not required.

    Primary Location

    : University

    Job Category

    : Clinical Research


    : 311500000 Neurology Chair Office

    Employee Status

    : Regular

    Shift: Day/1st Shift

    Work Arrangement (final schedule to be determined by the department/hiring manager): Hybrid Eligible

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