Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| n | 1 | Job Description: | n | 1 | The Department of Medicine, Division of Cardiology, has developed a clinical research infrastructure |
| > | within the Division. The goals are to increase industry-sponsored research, create a system that su | ||||
| > | pports physicians in operationalizing investigator-initiated studies, and develop a general cardiolo | ||||
| > | gy cohort study. | ||||
| 2 | The Department of Medicine, Division of Cardiology, has developed a clinical research infrastructure | ||||
| > | within the Division. The goals are to increase industry-sponsored research, create a system that su | ||||
| > | pports physicians in operationalizing investigator-initiated studies, and develop a general cardiolo | ||||
| > | gy cohort study. The purpose of this position is to carry out tasks as part of ongoing and future cl | ||||
| > | inical and translational research projects within the Division of Cardiology. Under the supervision | ||||
| > | of the Clinical Research Supervisor or Manager, the incumbent will perform duties related to the sup | ||||
| > | port and coordination of clinical studies and may receive training and development to prepare for ad | ||||
| > | vancement to the next level within the series. | ||||
| 3 | 2 | ||||
| t | 4 | Qualifications: | t | 3 | The purpose of this position is to carry out tasks as part of ongoing and future clinical and trans |
| > | lational research projects within the Division of Cardiology. Under the supervision of the Clinical | ||||
| > | Research Supervisor or Manager, the incumbent will perform duties related to the support and coordin | ||||
| > | ation of clinical studies and may receive training and development to prepare for advancement to the | ||||
| > | next level within the series. | ||||
| 5 | Required Qualifications: • HS graduate and sufficient experience and demonstrated skills to successf | ||||
| > | ully perform the assigned duties and responsibilities • Attention to detail; strong interpersonal sk | ||||
| > | ills; excellent, effective verbal and written communication skills to coordinate with subjects, team | ||||
| > | members, other departments and 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, c | ||||
| > | omplete projects in a timely manner, and prioritize multiple projects to ensure the completion of es | ||||
| > | sential tasks by deadlines. • Demonstrated ability to exercise tact and discretion in sensitive comm | ||||
| > | unications with patients and others. Demonstrated ability in handling a variety of confidential info | ||||
| > | rmation appropriately. • Demonstrated positive interpersonal skills and problem solving abilities. • | ||||
| > | Willing to travel (limited travel for investigator meetings) Preferred Qualifications: • Experience | ||||
| > | in clinical cardiology and clinical/cardiovascular research • Science, research, or medical backgro | ||||
| > | und • Applied knowledge in drug and/or device trials • A two-year commitment is preferred • Proficie | ||||
| > | ncy in the use of Committee of Human Research (CHR) online iMEDris system for submission, renewal, a | ||||
| > | nd modification of protocols through this system. • Understanding of patient population to create ra | ||||
| > | pport, while also giving insight to what is realistic and appropriate for patient participation. • I | ||||
| > | n-depth knowledge of ICH/GCP and FDA requirements for INDs, IDEs, and NDAs. • Experience in building | ||||
| > | strong working relationships with Sponsors, Monitors, PIs, and other key stakeholders • Experience | ||||
| > | with electronic medical records, EPIC preferred. • Knowledge of biospecimen collection, processing, | ||||
| > | and transport • Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelin | ||||
| > | es for research, confidentiality and HIPAA regulations, following the UCSF mission statement and pur | ||||
| > | pose for research, and a clear understanding of policies and procedures on patient safety and confid | ||||
| > | entiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge | ||||
| > | of medical terminology, research policies and guidelines, guidelines for packing/shipping infectiou | ||||
| > | s substances, database building/analysis, and data management within some of the following: Access, | ||||
| > | Stata, SASS/ SPSS, and Teleform programming platforms. • Certification by the Society of Clinical Re | ||||
| > | search Associates or the Association of Clinical Research Professionals • Experience applying the fo | ||||
| > | llowing regulations and guidelines: • Good Clinical Practice Guidelines • Health Information and Acc | ||||
| > | ountability Act (HIPAA) • The Protection of Human Research Subjects • CHR regulations for recruitmen | ||||
| > | t and consent of research subjects • Effective Cash Handling Procedures • Environmental Health and S | ||||
| > | afety Training • Fire/ Life Safety Training License / Certification: • No | ||||