Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| n | 1 | Job Description: | n | ||
| 2 | As a Clinical Research Coordinator, you will play a crucial role in managing and coordinating clinic | 1 | As a Clinical Research Coordinator, you will play a crucial role in managing and coordinating clinic | ||
| > | al research studies, ensuring their smooth execution and compliance with protocols and regulations. | > | al research studies, ensuring their smooth execution and compliance with protocols and regulations. | ||
| > | Working closely with the Director of Clinical Research and Principal Investigators, you will oversee | > | Working closely with the Director of Clinical Research and Principal Investigators, you will oversee | ||
| > | data collection, specimen management, and study results, contributing to the overall success of the | > | data collection, specimen management, and study results, contributing to the overall success of the | ||
| > | research initiatives. | > | research initiatives. | ||
| 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. - Exp | ||||
| > | erience with electronic medical records - Experience working with health professionals in a hospital | ||||
| > | and/or clinic setting - Experience working with patients in a health care setting - Experience as c | ||||
| > | linical research coordinator or research assistant - Attention to detail; strong interpersonal skill | ||||
| > | s; excellent, effective verbal and written communication skills to coordinate with subjects, team me | ||||
| > | mbers, other departments and outside institutions; and the ability to multi-task in a fast-paced env | ||||
| > | ironment while working with a diverse subject population. - Ability to work well independently, comp | ||||
| > | lete projects in a timely manner, and prioritize multiple projects to ensure the completion of essen | ||||
| > | tial tasks by deadlines. - Understanding of patient population to create rapport and a relationship, | ||||
| > | while also giving insight to what is realistic and appropriate for patient participation. Preferred | ||||
| > | Qualifications: - Bachelor or Associate degree in health-related field - Minimum three years’ exper | ||||
| > | ience as clinical research coordinator - SoCRA or other research professional certification - Biling | ||||
| > | ual (fluent in Spanish and English) - Knowledge of UCSF and departmental policies for dealing with r | ||||
| > | eimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mis | ||||
| > | sion statement and purpose for research, and a clear understanding of policies and procedures on pat | ||||
| > | ient safety and confidentiality (electronic and hard copy medical records, patient charts, communica | ||||
| > | tion, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for pack | ||||
| > | ing/shipping infectious substances, database building/analysis, and data management within some of t | ||||
| > | he following: Access, Stata, SASS/ SPSS, and Teleform programming platforms. - Experience applying t | ||||
| > | he following regulations and guidelines:- Good Clinical Practice Guidelines - Health Information and | ||||
| > | Accountability Act (HIPAA) - The Protection of Human Research Subjects - CHR regulations for recrui | ||||
| > | tment and consent of research subjects - Environmental Health and Safety Training | ||||