Clinical Research Coordinator I, Department of Neurology

University of Arizona

Tucson, United StatesFull time
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Location
Tucson, United States
Job type
Full time
Posted
Oct 16
4 days ago
Career path

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About the company

University of Arizona

Higher education · 11 to 50 employees

University of Arizona on LinkedIn

What you'll do

  • Recruit, screen, enroll, and assist research participants; collect and process study information and specimens.
  • Support protocol submissions, data collection and analysis, reporting, study documentation, and daily lab operations.

What you need

  • Requires the ability to manage multiple priorities, maintain accurate and detailed records, meet deadlines, and communicate effectively.
  • Must be able to work independently and with a team while upholding research integrity and ethical and compliance standards.

Key skills

research documentationdata entrywritten and verbal communicationmanage multiple prioritiesdata accuracyresearch integrityethical and compliance standards

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Read the full posting here
Following detailed instructions by the supervisor, assist with promoting/recruiting research participants for long-term clinical trials.Participate in routine recruitment, screening, and enrollment of study participants who meet research eligibility criteria. Help obtain consent forms for approval by Human Subjects Panel. Maintain and update recruitment and screening materials, compliance forms, and tracking documents.Assist with collecting basic information, such as medical histories and assessments interviews, collect and process specimens, answer general questions, fill out case report forms, and help with telephone and in-person contact. Notifies Principal Investigator and supervisor of subject status.Under the direction of the PI and Senior lab members, assist with new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies.Aid in the submission of study protocols and amendments, consent forms, and recruiting materials to the Institutional Review Board and department for approval with oversight from supervisor.Provide assistance with collecting data, entering and analyzing data, and compiling reports, adhering to proper research protocols. Prepare basic documentation, reports, graphs, and other materials. Keep appropriate logs, tracks participants, and prepares study materials.Under direction of the PI and Senior lab members, assist with coordinating and carrying out daily operations including ordering/maintaining laboratory supplies/equipment.Attend lab meetings. Knowledge, Skills & Abilities: Ability to manage multiple priorities, maintain accurate and detailed records, and meet deadlines in a fast-paced research environment.Strong written and verbal communication skills and proficiency with computer applications used for research documentation and data entry.Ability to work both independently and with a team, resolving issues with a positive outcome.Ability to maintain data accuracy, uphold research integrity, and perform work in accordance with ethical and compliance standards.Ability to contribute to the development of research programs, policies, and procedures and support continuous improvement.

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