University of California, San Francisco
Clinical Research Coordinator
University of California, San Francisco, San Francisco, California, United States, 94199
Overview
Neuro-Memory and Aging — Full Time — 86326BR
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.
Responsibilities
Support the management and coordination of tasks for single or multiple clinical research studies, depending on size and complexity.
Act as intermediary between services and departments while overseeing data and specimen management.
Manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports.
Coordinate staff work schedules, assist with training of Assistant CRCs, and assist the Clinical Research Supervisor and/or PI with oversight of other research staff.
Manage Investigator’s protocols in the Committee on Human Research online system, including renewals and modifications of protocol applications and implementation of new studies.
Participate in the review and writing of protocols to ensure IRB approval within University compliance; help assure compliance with all relevant regulatory agencies.
Oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation.
Maintain all regulatory documents; report study progress to investigators; participate in audits or reviews of study protocols; perform other duties as assigned.
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; strong interpersonal skills; excellent verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; 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 NA
About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences.
Benefits and Compensation The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.
Salary range: $34.32 - $55.19 (Hourly Rate).
To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
Department Description The UCSF Memory and Aging Center is an NIA-designated Alzheimer’s Disease Research Center (ADRC) working to translate research science into improved diagnosis and care for people with dementia due to Alzheimer’s disease and related diseases, as well as to find a treatment or prevention. The Clinical Research Coordinator will be working on the Frontotemporal Dementia: Genes, Images, and Emotions study led by Drs. Maria Luisa Gorno Tempini, Bill Seeley, and Howie Rosen. The purpose of this study is to help understand the clinical, genetic, imaging, emotional and diagnostic features of frontotemporal dementia (FTD). The study collects longitudinal clinical, imaging, behavioral and autopsy data to be analyzed with the goal of improving clinical care for patients with FTD.
Employment Details
Job Type: Full-time
Location: San Francisco, CA (Mission Bay)
Work Style: Fully On-Site
Shift: Days, 8 Hours; Monday - Friday, 8:00am - 5:00pm
Legal and Equality The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
Join us to find a rewarding career contributing to improving healthcare worldwide.
#J-18808-Ljbffr
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.
Responsibilities
Support the management and coordination of tasks for single or multiple clinical research studies, depending on size and complexity.
Act as intermediary between services and departments while overseeing data and specimen management.
Manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports.
Coordinate staff work schedules, assist with training of Assistant CRCs, and assist the Clinical Research Supervisor and/or PI with oversight of other research staff.
Manage Investigator’s protocols in the Committee on Human Research online system, including renewals and modifications of protocol applications and implementation of new studies.
Participate in the review and writing of protocols to ensure IRB approval within University compliance; help assure compliance with all relevant regulatory agencies.
Oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation.
Maintain all regulatory documents; report study progress to investigators; participate in audits or reviews of study protocols; perform other duties as assigned.
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; strong interpersonal skills; excellent verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; 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 NA
About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences.
Benefits and Compensation The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.
Salary range: $34.32 - $55.19 (Hourly Rate).
To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
Department Description The UCSF Memory and Aging Center is an NIA-designated Alzheimer’s Disease Research Center (ADRC) working to translate research science into improved diagnosis and care for people with dementia due to Alzheimer’s disease and related diseases, as well as to find a treatment or prevention. The Clinical Research Coordinator will be working on the Frontotemporal Dementia: Genes, Images, and Emotions study led by Drs. Maria Luisa Gorno Tempini, Bill Seeley, and Howie Rosen. The purpose of this study is to help understand the clinical, genetic, imaging, emotional and diagnostic features of frontotemporal dementia (FTD). The study collects longitudinal clinical, imaging, behavioral and autopsy data to be analyzed with the goal of improving clinical care for patients with FTD.
Employment Details
Job Type: Full-time
Location: San Francisco, CA (Mission Bay)
Work Style: Fully On-Site
Shift: Days, 8 Hours; Monday - Friday, 8:00am - 5:00pm
Legal and Equality The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
Join us to find a rewarding career contributing to improving healthcare worldwide.
#J-18808-Ljbffr