Senior Clinical Research Coordinator job at University of California in Los Angeles, CA
Title: Sr. Clinical Research Coordinator - Radiation Oncology
Location: Los Angeles United States
Job Description:
General Information
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Work Location: Los Angeles, CA, USA
Onsite or Remote
Fixed Hybrid
Work Schedule
Monday through Friday; 8:00am to 5:00pm; hours may vary.
Salary Range: $6892.14 - 11089.02 Monthly
Employment Type
2 - Staff: Career
Duration
Indefinite
Job #
28364
Primary Duties and Responsibilities
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Life-saving breakthroughs, innovative therapies, and next-generation technologies. Through vision, tenacity, and inspiration, UCLA Health's world-class researchers are redefining human health and patient care. Join us and live out your passion for discovery while making an incredible difference in the lives of people around the world.
The Senior Clinical Research Coordinator oversees the operational management of clinical research studies from start-up through closeout. This role is well-suited for an experienced research professional who can lead study activities, manage priorities, and ensure high-quality, compliant execution across complex research projects.
Key Responsibilities:
Manage day-to-day operations for one or more clinical research studies, including multicenter and investigator-initiated trials
Ensure study protocols and procedures are carried out accurately, safely, and on schedule
Coordinate timelines, prioritize tasks, and support project management needs
Train and supervise research staff as needed
Collaborate with Principal Investigators, sponsors, and internal and external partners on compliance, financial, and operational aspects of studies
Salary: $6,892.14 - $11,089.02 monthly
Job Qualifications
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Required:
Bachelor's Degree or three-to seven years of study coordination or clinical research coordination experience
Ability to work flexible hours to accommodate research deadlines.
Strong interpersonal communication skills to effectively and diplomatically interact with others, including institutional leadership.
Strong written communication skills, ability to compose advanced correspondence and manage large file systems.
Advanced typing and computer skill/ability including word-processing, use of spreadsheets, email and data entry.
Sufficient math ability and knowledge of clinical trials budgeting processes to manage the preparation of clinical trial budgets.
Advance knowledge of the clinical research regulatory framework and institutional requirements.
Ability to supervise and delegate clerical work as needed.
Advanced knowledge of Good Clinical Practice (GCP) for clinical research.
Preferred:
Working knowledge of FDA applications
As a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer.
Current/former UC employees are subject to a personnel file review.
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Location: Los Angeles United States
Job Description:
General Information
Press space or enter keys to toggle section visibility
Work Location: Los Angeles, CA, USA
Onsite or Remote
Fixed Hybrid
Work Schedule
Monday through Friday; 8:00am to 5:00pm; hours may vary.
Salary Range: $6892.14 - 11089.02 Monthly
Employment Type
2 - Staff: Career
Duration
Indefinite
Job #
28364
Primary Duties and Responsibilities
Press space or enter keys to toggle section visibility
Life-saving breakthroughs, innovative therapies, and next-generation technologies. Through vision, tenacity, and inspiration, UCLA Health's world-class researchers are redefining human health and patient care. Join us and live out your passion for discovery while making an incredible difference in the lives of people around the world.
The Senior Clinical Research Coordinator oversees the operational management of clinical research studies from start-up through closeout. This role is well-suited for an experienced research professional who can lead study activities, manage priorities, and ensure high-quality, compliant execution across complex research projects.
Key Responsibilities:
Manage day-to-day operations for one or more clinical research studies, including multicenter and investigator-initiated trials
Ensure study protocols and procedures are carried out accurately, safely, and on schedule
Coordinate timelines, prioritize tasks, and support project management needs
Train and supervise research staff as needed
Collaborate with Principal Investigators, sponsors, and internal and external partners on compliance, financial, and operational aspects of studies
Salary: $6,892.14 - $11,089.02 monthly
Job Qualifications
Press space or enter keys to toggle section visibility
Required:
Bachelor's Degree or three-to seven years of study coordination or clinical research coordination experience
Ability to work flexible hours to accommodate research deadlines.
Strong interpersonal communication skills to effectively and diplomatically interact with others, including institutional leadership.
Strong written communication skills, ability to compose advanced correspondence and manage large file systems.
Advanced typing and computer skill/ability including word-processing, use of spreadsheets, email and data entry.
Sufficient math ability and knowledge of clinical trials budgeting processes to manage the preparation of clinical trial budgets.
Advance knowledge of the clinical research regulatory framework and institutional requirements.
Ability to supervise and delegate clerical work as needed.
Advanced knowledge of Good Clinical Practice (GCP) for clinical research.
Preferred:
Working knowledge of FDA applications
As a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer.
Current/former UC employees are subject to a personnel file review.
Apply tot his job
Apply To this Job