Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| n | 1 | Job Description: | n | ||
| 2 | The Clinical Research Coordinator will work independently or under general direction by the Clinical | 1 | The Clinical Research Coordinator will work independently or under general direction by the Clinical | ||
| > | Research Supervisor and/or Principal Investigator (PI) to manage and coordinate research protocols | > | Research Supervisor and/or Principal Investigator (PI) to manage and coordinate research protocols | ||
| > | within the Department of Surgery Clinical Research Core. The coordinator will be assigned studies ac | > | within the Department of Surgery Clinical Research Core. The coordinator will be assigned studies ac | ||
| > | ross the 7 divisions in the department based on Principal Investigator needs; may coordinate the dat | > | ross the 7 divisions in the department based on Principal Investigator needs; may coordinate the dat | ||
| > | a collection and operations of several concurrent clinical research studies under the guidelines of | > | a collection and operations of several concurrent clinical research studies under the guidelines of | ||
| > | research protocols, UCSF and regulating agency policies. | > | research protocols, UCSF and regulating agency policies. | ||
| t | 3 | t | |||
| 4 | Qualifications: | ||||
| 5 | Required Qualifications: - HS graduation and sufficient experience and demonstrated skills to succes | ||||
| > | sfully perform the assigned duties and responsibilities; and/or equivalent experience/training. - At | ||||
| > | tention to detail and accuracy; strong interpersonal skills; excellent, effective verbal and written | ||||
| > | communication skills to coordinate with patients, team members, other departments, outside institut | ||||
| > | ions, and companies. - Ability to multitask in a fast-paced environment while working with a diverse | ||||
| > | population and competing deadlines. - Ability to work well independently and in a team setting, tak | ||||
| > | e initiative, complete projects in a timely manner, and prioritize multiple responsibilities to ensu | ||||
| > | re the completion of essential tasks by deadlines. Preferred Qualifications: - BA/BS with biology or | ||||
| > | public health coursework included. - Knowledge of medical terminology. - Experience with electronic | ||||
| > | medical records. - Experience with research tools such as REDCap and Qualtrics. - Prior analytical | ||||
| > | and writing skills in a science/research environment. - Understanding of patient population to creat | ||||
| > | e rapport and a relationship, while giving insight into what is realistic and appropriate for patien | ||||
| > | t participation. - Fluency in the usage of the Institutional Review Board (IRB) online systems for t | ||||
| > | he submission, renewal, and modification of research protocols. - Certification by the Society of Cl | ||||
| > | inical Research Associates or the Association of Clinical Research Professionals. - Knowledge of UCS | ||||
| > | F and departmental policies for dealing with research payments and reimbursements; patient safety an | ||||
| > | d confidentiality; packing/shipping infectious substances; database building/analysis, and data mana | ||||
| > | gement within some of the following platforms: Access, Stata, SASS/ SPSS, and Teleform. - Experience | ||||
| > | applying the following regulations and guidelines:- The Protection of Human Research Subjects - Goo | ||||
| > | d Clinical Practice - Health Insurance Portability and Accountability Act (HIPAA) - IRB regulations | ||||
| > | - Safe shipping practices (IATA) - Environmental Health and Safety Training - Fire Safety Training. | ||||