Clinical Research Coordinator I

4 weeks ago

Tucson, United States University of Arizona Full time

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. Notify 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, track participants, and prepare 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, and Abilities

Knowledge about neurological disorders including movement disorders (e.g., Parkinson's disease), seizure disorders (e.g., epilepsy syndromes), and vascular neurological disorders. Passion for neurological research and development of treatments for neurological disorders.Motivated to provide high quality, compliant research.Skill in maintaining detailed records.Desire to build new program and develop new policies.Ability to work both independently and with a team, resolving issues with a positive outcome.High level of integrity, ethics, and professionalism.Strong communication and computer skills.Strong organization skills and significant attention to detail for data entry.

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    1 month ago

    Tucson, United States University of Arizona Full time

    Screen, recruit, and enroll participants for medical studies by interviewing potential participants and reviewing medical history to determine if eligibility requirements are met.Evaluate potential study participants to ensure they meet eligibility requirements, instruct study participants concerning research protocol, and complete the patient informed...

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