Skip to content

General Information

Job Name
Clinical Research Coordinator (Spanish)
Department
1383350 - M MED CORE DGIM
Position type
Full Time
Workplace
Flexible 4 Days On-Site
Primary Location
San Francisco, CA, United States
Job ID
CONV_88350BR

Description & Requirements

Job Description
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 directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
Qualifications
Required Qualifications: - Spanish language proficiency – reading, writing, and speaking - HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training. - Attention to detail; strong interpersonal skills; 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, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines. Preferred Qualifications: - Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system. - Understanding of patient 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 Associates or the Association of Clinical Research Professionals - Experience with electronic medical records. - Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, 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 confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms. - Experience applying the following regulations and guidelines: - 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 Safety Training

Additional Details

Job Code
CLIN RSCH CRD (009335)
Assignment Category
Career
IAP Level
None
Job Family
Research and Laboratory
Campus 1
Mission Bay (SF)
Campus 2
Mission Bay (SF)
Campus 3
Mission Bay (SF)
Percentage (%)
100
Shift Length
8 hours
Shift Type
Day
Bargaining Unit
RX
Additional Shift Details
Monday - Friday, flexible 3 days onsite
Go back

Similar jobs

View all