Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| n | 1 | Job Description: | n | 1 | We are seeking a highly motivated Clinical Research Coordinator to join the brain imaging groups of |
| > | Dr. Yan Li and Dr. Janine Lupo at the UCSF Department of Radiology and Biomedical Imaging. The ideal | ||||
| > | candidate will play a pivotal role in coordinating research brain imaging studies. This position re | ||||
| > | quires a strong background in coordination, preferably with experience working directly with clinica | ||||
| > | l research coordination. | ||||
| 2 | We are seeking a highly motivated Clinical Research Coordinator to join the brain imaging groups of | ||||
| > | Dr. Yan Li and Dr. Janine Lupo at the UCSF Department of Radiology and Biomedical Imaging. The ideal | ||||
| > | candidate will play a pivotal role in coordinating research brain imaging studies. This position re | ||||
| > | quires a strong background in coordination, preferably with experience working directly with clinica | ||||
| > | l research coordination. The Clinical Research Coordinator will perform independently or with genera | ||||
| > | l direction at the fully operational journey level of the series to execute, manage, and coordinate | ||||
| > | research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (P | ||||
| > | I); may coordinate the data collection and operations of several concurrent clinical research studie | ||||
| > | s under the guidelines of research protocols, UCSF and regulating agency policies. Incumbent’s dutie | ||||
| > | s may include, but will not be limited to supporting the management and coordinating the tasks of mu | ||||
| > | ltiple clinical research studies, depending on their size and complexity; act as intermediary betwee | ||||
| > | n services and departments while overseeing data and specimen management; enroll and consent patient | ||||
| > | s into research studies; manage and report on study results; create, clean, update, and manage datab | ||||
| > | ases and comprehensive datasets and reports; coordinate staff work schedules, assist with training o | ||||
| > | f staff/learners, and assist Clinical Research Supervisor and/or PI with oversight of other research | ||||
| > | staff; manage Investigator’s protocols in the Committee on Human Research online system, as well as | ||||
| > | renewals and modifications of protocol applications and the implementation of new studies; particip | ||||
| > | ate in the review and writing of protocols to ensure institutional review board approval within Univ | ||||
| > | ersity compliance; help assure compliance with all relevant regulatory agencies; oversee study data | ||||
| > | integrity; implement and maintain periodic quality control procedures; interface with departments to | ||||
| > | obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study pro | ||||
| > | gress to investigators; participate in any internal and external audits or reviews of study protocol | ||||
| > | s; and perform other duties as assigned. | ||||
| 3 | 2 | ||||
| t | 4 | Qualifications: | t | 3 | The Clinical Research Coordinator will perform independently or with general direction at the fully |
| > | operational journey level of the series to execute, manage, and coordinate research protocols, as d | ||||
| > | irected by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the d | ||||
| > | ata collection and operations of several concurrent clinical research studies under the guidelines o | ||||
| > | f research protocols, UCSF and regulating agency policies. | ||||
| 5 | Required Qualifications: - High School Diploma or equivalent experience - Excellent organizational s | 4 | |||
| > | kills, multi-tasking, and attention to detail; strong interpersonal skills; excellent, effective ver | ||||
| > | bal and written communication skills to coordinate with subjects, team members, other departments an | ||||
| > | d outside institutions; and the ability to multi-task in a fast-paced environment while working with | ||||
| > | a diverse subject population - Ability to work well independently, complete projects in a timely ma | ||||
| > | nner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines - Ab | ||||
| > | ility to work well with patients and demonstrate patience, respect, and compassion to study particip | ||||
| > | ants and their families Preferred Qualifications: - BCBA certification or experience working with cl | ||||
| > | inical research imaging studies - Bachelor's degree in neuroscience, biology, biomedical imaging, ap | ||||
| > | plied math, engineering, or a related field (Master's degree preferred) - Experience with brain imag | ||||
| > | ing data processing techniques and/or programming skills is desirable - Proficiency in Matlab, Pytho | ||||
| > | n, statistical analysis software (e.g. SPSS, R) - Fluency in the usage of the Committee of Human Res | ||||
| > | earch (CHR) online iMEDris system for submission, renewal, and modification of protocols through thi | ||||
| > | s system - Understanding of patient population to create rapport and a relationship, while also givi | ||||
| > | ng insight to what is realistic and appropriate for patient participation - Experience with electron | ||||
| > | ic medical records - Knowledge of UCSF and departmental policies for dealing with reimbursement, gui | ||||
| > | delines for research, confidentiality and HIPPA regulations, following the UCSF mission statement an | ||||
| > | d purpose for research, and a clear understanding of policies and procedures on patient safety and c | ||||
| > | onfidentiality (electronic and hard copy medical records, patient charts, communication, etc.); know | ||||
| > | ledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infe | ||||
| > | ctious substances, database building/analysis, and data management within some of the following: Acc | ||||
| > | ess, Stata, SASS/ SPSS, and Teleform programming platforms - Experience applying the following regul | ||||
| > | ations and guidelines:- Good Clinical Practice Guidelines - Health Information and Accountability Ac | ||||
| > | t (HIPAA) - The Protection of Human Research Subjects - CHR regulations for recruitment and consent | ||||
| > | of research subjects - Effective Cash Handling Procedures - Environmental Health and Safety Training | ||||
| > | - Fire Safety Training | ||||
| 5 | Incumbent’s duties may include, but will not be limited to supporting the management and coordinati | ||||
| > | ng the tasks of multiple clinical research studies, depending on their size and complexity; act as i | ||||
| > | ntermediary between services and departments while overseeing data and specimen management; enroll a | ||||
| > | nd consent patients into research studies; manage and report on study results; create, clean, update | ||||
| > | , and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assi | ||||
| > | st with training of staff/learners, and assist Clinical Research Supervisor and/or PI with oversight | ||||
| > | of other research staff; manage Investigator’s protocols in the Committee on Human Research online | ||||
| > | system, as well as renewals and modifications of protocol applications and the implementation of new | ||||
| > | studies; participate in the review and writing of protocols to ensure institutional review board ap | ||||
| > | proval within University compliance; help assure compliance with all relevant regulatory agencies; o | ||||
| > | versee study data integrity; implement and maintain periodic quality control procedures; interface w | ||||
| > | ith departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents | ||||
| > | ; report study progress to investigators; participate in any internal and external audits or reviews | ||||
| > | of study protocols; and perform other duties as assigned. | ||||