Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| n | 1 | Job Description: | n | 1 | The Department of Otolaryngology - Head & Neck Surgery is recruiting an Assistant Clinical Research |
| > | Coordinator (ACRC) for the Childern's Communication Center (CCC). | ||||
| 2 | The Department of Otolaryngology - Head & Neck Surgery is recruiting an Assistant Clinical Research | ||||
| > | Coordinator (ACRC) for the Childern's Communication Center (CCC). Under the supervision of a Clinica | ||||
| > | l Research Supervisor, the incumbent will perform entry-level duties related to the support and coor | ||||
| > | dination of clinical research and outreach activities and may receive training and development to pr | ||||
| > | epare and advance for journey-level work at the next level within the series. Duties will include, b | ||||
| > | ut will not be limited to the following: Assistance with coordination and in-person participation in | ||||
| > | on-site and off-site CCC clinical research andoutreach activities. Telephone survey administration | ||||
| > | Database management and data entry while maintaining data quality Review of medical charts and elect | ||||
| > | ronic records to extract medical information and other data for use in studies Help with the recruit | ||||
| > | ment, enrollment, registration, scheduling, and retention of study participants Assistance to resear | ||||
| > | ch personnel to keep patients on study schedules Administrative support for research study activity | ||||
| > | (including working with the UCSF Committee for Human Research and other regulatory agencies) Perform | ||||
| > | ance of other duties as assigned | ||||
| 3 | 2 | ||||
| t | 4 | Qualifications: | t | 3 | Under the supervision of a Clinical Research Supervisor, the incumbent will perform entry-level dut |
| > | ies related to the support and coordination of clinical research and outreach activities and may rec | ||||
| > | eive training and development to prepare and advance for journey-level work at the next level within | ||||
| > | the series. | ||||
| 5 | Required Qualifications: - HS graduation and sufficient experience and demonstrated skills to succes | 4 | |||
| > | sfully perform the assigned duties and responsibilities; and/or equivalent experience/training. - Co | ||||
| > | mputer experience: Microsoft applications, FileMaker pro, REDCap, video and photo editing software - | ||||
| > | Demonstrate attention to detail, complete projects on time, prioritize multiple tasks to meet deadl | ||||
| > | ines, collaborate effectively with team members, adapt to changing priorities, and communicate clear | ||||
| > | ly Preferred Qualifications: - 1-3 years of experience working with children ages 0-18 years in a cl | ||||
| > | assroom or clinical setting - At least 1 year of experience working with deaf/hard-of-hearing childr | ||||
| > | en and their families - Proficiency in a second language (Spanish or Cantonese) - Fluency in the usa | ||||
| > | ge of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modificat | ||||
| > | ion of protocols through this system. - Understanding the patient population to create rapport and a | ||||
| > | relationship while also giving insight into what is realistic and appropriate for patient participa | ||||
| > | tion. - Experience with electronic medical records. - Experience with REDCap database structure, mai | ||||
| > | ntenance, management and/or creation - Knowledge of UCSF and departmental policies for dealing with | ||||
| > | reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mi | ||||
| > | ssion statement and purpose for research, and a clear understanding of policies and procedures on pa | ||||
| > | tient safety and confidentiality (electronic and hard copy medical records, patient charts, communic | ||||
| > | ation, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for pac | ||||
| > | king/shipping infectious substances, database building/analysis, and data management within some of | ||||
| > | the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms. - Knowledge of medical | ||||
| > | terminology, research policies and guidelines - Prior experience as a teacher of children with spec | ||||
| > | ial needs - Experience applying the following regulations and guidelines: Good Clinical Practice Gui | ||||
| > | delines Health Information and Accountability Act (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 | Duties will include, but will not be limited to the following: | ||||
| 6 | |||||
| 7 | * | ||||
| 8 | |||||
| 9 | Assistance with coordination and in-person participation in on-site and off-site CCC clinical resea | ||||
| > | rch andoutreach activities. | ||||
| 10 | * | ||||
| 11 | |||||
| 12 | Database management and data entry while maintaining data quality | ||||
| 13 | * | ||||
| 14 | |||||
| 15 | Review of medical charts and electronic records to extract medical information and other data for u | ||||
| > | se in studies | ||||
| 16 | * | ||||
| 17 | |||||
| 18 | Help with the recruitment, enrollment, registration, scheduling, and retention of study participant | ||||
| > | s | ||||
| 19 | * | ||||
| 20 | |||||
| 21 | Assistance to research personnel to keep patients on study schedules | ||||
| 22 | * | ||||
| 23 | |||||
| 24 | Administrative support for research study activity (including working with the UCSF Committee for H | ||||
| > | uman Research and other regulatory agencies) | ||||
| 25 | * | ||||
| 26 | |||||
| 27 | Performance of other duties as assigned | ||||