Clinical Research Coordinator I

University of Arizona

  • Tucson, AZ
  • 30+ days ago

    Highlights

    Communicate study related issues to investigators, sponsors, coordinating centers, study coordinators, clinical team, managers, and other institutions in a timely fashion. Participate in preparation, review, submission, and maintenance of regulatory activities/submissions, ensure accuracy and timeliness to all collaborative parties.

    Numbers & Facts

    LocationTucson, AZ

    Description

    • Maintain awareness of status of all active studies.
    • Participate in development and implementation of associated projects under the guidance of the research director.
    • Identify potentially eligible participants.
    • Conduct remote consent according to protocol specifications.
    • Conduct pre-consent screening procedures according to protocol specifications to determine eligibility.
    • Execute the informed consent process according to Good Clinical Practices (GCP), procedures and other applicable policies.
    • Develop a rapport with study participants.
    • Collaborate effectively with others to ensure proper progress and completion of studies.
    • Conduct data entry and validation to ensure accuracy, quality, and compliance of the data collection process.
    • Maintain the master database files for clinical research protocols.
    • Document in applicable systems (tracking, electronic health, etc.) participants approached, screened, and enrolled in the study.
    • Maintain detailed records.
    • Compose clear, precise, and detailed correspondence.
    • Communicate study related issues to investigators, sponsors, coordinating centers, study coordinators, clinical team, managers, and other institutions in a timely fashion.
    • Communicate with participants' clinical team regarding study participation as indicated by protocol and/or manual of operations.
    • Communicate challenges with recruitment and retention to the study leadership.
    • Participate in preparation, review, submission, and maintenance of regulatory activities/submissions, ensure accuracy and timeliness to all collaborative parties.
    • Prepare for and participate in monitor visits, audits, and quality reviews (internal and external) in a professional manner.

    Knowledge, Skills, and Abilities:

    • Knowledge of the principles, practices, and techniques of research clinical skills.
    • Skill in completing tasks with attention to detail.
    • Skill in using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions, and approaches to problems.
    • Skill in talking to others to convey information effectively.
    • Ability to manage multiple concurrent deadlines.
    • Ability to accurately prepare and maintain records, files, and reports.
    • Ability to handle difficult and stressful situations with professional composure.
    • Ability to understand and follow instructions.
    • Ability to exercise sound judgment in making critical decisions.
    • Ability to work evenings, overnights, and weekends.

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