Job Description
Description
The Semel Institute is seeking to hire a full time Assistant Clinical Research Coordinator to complete the duties of AIMS Research Assessor & Screener. In this role you will report to the Principal Investigator and will be responsible for conducting research activities as a part of a clinical research study involving patient contact, obtaining consent, and collection of psychological.
Duties Of This Role Can Include
- Recruitment – Coordinate & maintain subject recruitment strategies:
- Assisting with maintaining the flow of subject participants into study to ensure subject pool sufficient to meet study’s recruitment objectives.
- Screening and Subject eligibility:
- Person will participate in outreach to clinical and community sites to recruit participants;
- Person will serve as a study assessor; including conducting screening for eligibility and baseline assessments;
- Person will undergo the study assessor trainings and inter-rater reliability testing before certification to assess in this study;
- Person will review informed consent and eligibility procedures with study participants;
- Person will conduct subject interviews including administration of standardized study questionnaires and instruments using all of the diagnostic / interview-based instruments that we propose in this study (GRID Hamilton Depression Rating Scale, Columbia Suicide Severity Rating Scale, Scale for Suicide Ideation).
- Follow-up assessment
- Coordinate scheduling of assessment visits
- Complete follow-up assessments including interviews as noted above
- Maintain confidentiality and non-judgmental attitude regarding study participants when reviewing questionnaire responses for accuracy, completeness, and appropriateness.
- Maintain flow of subjects into study adequate to meeting enrollment targets.
- Maintain subject adherence over course of a longitudinal follow-up period.
- Research Administrative & Data Management Tasks
- Schedule participant baseline and follow-up assessments
- Generate and oversee all communication with study participants.
- Prepare necessary data forms for study participants.
- Assist in maintaining subject files throughout project.
- Assist in maintaining study participant tracking files.
- Assist in maintaining current subject scheduling
- Assist in maintain working relationship with statisticians regarding subject recruitment, data collection, and reports; data cleaning; tracking of missing and completed data; data entry.
Pay Range: $27.08 – $43.55 hourlyQualifications
Required
- Demonstrated skills with clinical and non-clinical subject recruitment,
- Demonstrated skills in working with older adult populations,
- Experience in interviewing subjects via telephone and in person about sensitive topics, such as medical history, depression, substance dependence, and family history of same,
- Demonstrated skills in questionnaire administration, avoiding judgment and bias,
- Experience with Word, Excel and PowerPoint,
- Ability to independently compose appropriate and grammatically correct correspondence,
- Ability to work independently, to follow instructions, and to work cooperatively with other staff members and other research groups/services,
- Ability to sensitively, effectively, and discretely handle confidential data and subject information,
- Excellent interpersonal skills necessary for maintaining study integrity and credibility with physicians, office staff, medical staff, and subject,
- Ability to work under multiple deadlines and complete work in a timely manner
Preferred
- Minimum of Bachelor’s degree with major in psychology or allied field,
- Familiarity with research involving human subject contact, consent procedures, data collection, and data tracking,
- Demonstrated skills in structured clinical interviews for psychiatric diagnosis.
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