Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| n | 1 | Job Description: | n | 1 | 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 di | ||||
| > | rected by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the da | ||||
| > | ta collection and operations of several concurrent clinical research studies under the guidelines of | ||||
| > | research protocols, UCSF and regulating agency policies. | ||||
| 2 | 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 di | ||||
| > | rected by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the da | ||||
| > | ta collection and operations of several concurrent clinical research studies under the guidelines of | ||||
| > | research protocols, UCSF and regulating agency policies. Incumbent’s duties may include, but will n | ||||
| > | ot be limited to supporting the management and coordinating the tasks of single or multiple clinical | ||||
| > | research studies, depending on their size and complexity; act as intermediary between services and | ||||
| > | departments while overseeing data and specimen management; manage and report on study results; creat | ||||
| > | e, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work | ||||
| > | schedules, assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or P | ||||
| > | I 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 imple | ||||
| > | mentation of new studies; participate in the review and writing of protocols to ensure institutional | ||||
| > | review board approval within University compliance; help assure compliance with all relevant regula | ||||
| > | tory agencies; oversee study data integrity; implement and maintain periodic quality control procedu | ||||
| > | res; interface with departments to obtain UCSF approval prior to study initiation; maintain all regu | ||||
| > | latory documents; report study progress to investigators; participate in any internal and external a | ||||
| > | udits or reviews of study protocols; and perform other duties as assigned. | ||||
| 3 | 2 | ||||
| t | 4 | Qualifications: | t | 3 | Incumbent’s duties may include, but will not be limited to supporting the management and coordinati |
| > | ng the tasks of single or multiple clinical research studies, depending on their size and complexity | ||||
| > | ; act as intermediary between services and departments while overseeing data and specimen management | ||||
| > | ; manage and report on study results; create, clean, update, and manage databases and comprehensive | ||||
| > | datasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs, and a | ||||
| > | ssist Clinical Research Supervisor and/or PI with oversight of other research staff; manage Investig | ||||
| > | ator’s protocols in the Committee on Human Research online system, as well as renewals and modificat | ||||
| > | ions of protocol applications and the implementation of new studies; participate in the review and w | ||||
| > | riting of protocols to ensure institutional review board approval within University compliance; help | ||||
| > | assure compliance with all relevant regulatory agencies; oversee study data integrity; implement an | ||||
| > | d maintain periodic quality control procedures; interface with departments to obtain UCSF approval p | ||||
| > | rior 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 du | ||||
| > | ties as assigned. | ||||
| 5 | Required Qualifications - HS graduation and sufficient experience and demonstrated skills to success | ||||
| > | fully perform the assigned duties and responsibilities; and/or equivalent experience/training. - Att | ||||
| > | ention to detail; strong interpersonal skills; excellent, effective verbal and written communication | ||||
| > | skills to coordinate with subjects, team members, other departments and outside institutions; and t | ||||
| > | he 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 manner, and prioritize multipl | ||||
| > | e projects to ensure the completion of essential tasks by deadlines. - Previous CRC experience Prefe | ||||
| > | rred Qualifications - Fluency in the usage of Committee of Human Research (CHR) online iMEDris syste | ||||
| > | m for submission, renewal, and modification of protocols through this system. - Understanding of pat | ||||
| > | ient population to create rapport and a relationship, while also giving insight to what is realistic | ||||
| > | and appropriate for patient participation. - Certification by the Society of Clinical Research Asso | ||||
| > | ciates or the Association of Clinical Research Professional - Experience with electronic medical rec | ||||
| > | ords. - Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for r | ||||
| > | esearch, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for | ||||
| > | research, and a clear understanding of policies and procedures on patient safety and confidentialit | ||||
| > | y (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medi | ||||
| > | cal terminology, research policies and guidelines, guidelines for packing/shipping infectious substa | ||||
| > | nces, database building/analysis, and data management within some of the following: Access, Stata, S | ||||
| > | ASS/ SPSS, and Teleform programming platforms. - Experience applying the following regulations and g | ||||
| > | uidelines:- Good Clinical Practice Guidelines - 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 Safe | ||||
| > | ty Training | ||||