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Clinical Research Coordinator I | University of California San Diego


University of California San Diego


Location

La Jolla, CA | United States


Job description

This is a UC San Diego Internal Recruitment open to UCSD and UCSD Health System Staff Only

UCSD Layoff from Career Appointment : Apply by 02/01/2024 for consideration with preference for rehire. All layoff applicants should contact their Employment Advisor.

Special Selection Applicants : Apply by 02/06/2024. Eligible Special Selection clients should contact their Disability Counselor for assistance.

DESCRIPTION

Within the Department of Pathology, the Pandemic Applications Laboratory and Microbiology Service (PALMS) performs a number of clinical research studies. Many of these research studies are funded by the NIH and other industry sponsors. The laboratory is situated at the Center for Advanced Laboratory Medicine where most of the laboratory testing for UCSD associated hospitals takes place. The laboratory also is associated with the Center for Innovative Phage Applications and Therapeutics (IPATH) and Dr. Pride's research laboratory in the Department of Pathology, which is dedicated to bacteriophage and human virome/microbiome analysis on UCSD main campus. There also are clinical research studies that sometimes are run out of the IPATH laboratory and Dr. Pride's research laboratory from main campus. Each of the three research entities cooperate under single leadership to advance research goals within the Department of Pathology.

The individual will be responsible for coordinating all of the research studies taking place at the PALMS laboratory as well as all of the clinical research studies taking place in the IPATH laboratory and the basic research laboratory. The individual also will take on the responsibility of managing the basic research laboratory and will be responsible for ordering all of the supplies necessary for continuing ongoing research studies. They will be responsible for maintaining laboratory safety and ensuring that all laboratory staff at each location are up to date with safety training. The research coordinator will be responsible for maintaining regular contact with study sponsors and keeping track of study procedures. They also will be responsible for managing regulatory documents and assuring compliance with state and federal regulatory guidelines. The Clinical Research Coordinator may plan, develop, and implement start-up procedures for research studies, as well as lead, direct, and help to coordinate operational efforts, assure compliance with state and federal regulatory guidelines, oversee the quality of the medical and clinical research data, provide direction and guidance to investigators, provide education and information to the general public concerning the ongoing clinical trials, assist PIs with proposals, progress reports and manuscripts, independently create original documents and policies, and work closely with federal and state regulatory officials when/if indicated. Other duties assigned as needed.

MINIMUM QUALIFICATIONS


Job tags

Work experience placement


Salary

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