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General Information

Job Name
Clinical Research Coordinator Surgery
Department
1482000 - M Surgery
Position type
Full Time
Workplace
Fully On-Site
Primary Location
San Francisco, CA, United States
Job ID
CONV_88341BR

Description & Requirements

Job Description
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 within the Department of Surgery Clinical Research Core. The coordinator will be assigned studies across the 7 divisions in the department based on Principal Investigator needs; 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: - HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training. - Attention to detail and accuracy; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with patients, team members, other departments, outside institutions, 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, take initiative, complete projects in a timely manner, and prioritize multiple responsibilities to ensure 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 create rapport and a relationship, while giving insight into what is realistic and appropriate for patient participation. - Fluency in the usage of the Institutional Review Board (IRB) online systems for the submission, renewal, and modification of research protocols. - Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals. - Knowledge of UCSF and departmental policies for dealing with research payments and reimbursements; patient safety and confidentiality; packing/shipping infectious substances; database building/analysis, and data management 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 - Good Clinical Practice - Health Insurance Portability and Accountability Act (HIPAA) - IRB regulations - Safe shipping practices (IATA) - 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
Pamassus Heights (SF)
Campus 2
Pamassus Heights (SF)
Campus 3
Pamassus Heights (SF)
Percentage (%)
100
Shift Length
8 hours
Shift Type
Day
Bargaining Unit
RX
Additional Shift Details
Monday-Friday: 8:00 am - 5:00 pm / occasional after work hours
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