Clinical Research Coordinator job at University of California in Los Angeles, CA
Title: Clinical Research Coordinator
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
Flexible Hybrid
Work Schedule
Monday-Friday 8am-5pm
Salary Range: $35.31 - 56.82 Hourly
Employment Type
2 - Staff: Career
Duration
Indefinite
Job #
28463
Primary Duties and Responsibilities
Press space or enter keys to toggle section visibility
The Department of Medicine is seeking a Clinical Research Coordinator to support the full lifecycle of clinical research studies, from study design and start-up through conduct and closeout. The incumbent will be responsible for implementing and coordinating research activities for one or more studies, managing day-to-day operations, and prioritizing tasks to ensure milestones and deadlines are met.
Working closely with the Principal Investigator and a wide range of internal and external partners, the Clinical Research Coordinator will ensure studies are conducted in compliance with institutional policies, FDA regulations, and ICH Good Clinical Practice (GCP). Responsibilities include study coordination, regulatory compliance, financial and operational oversight, and collaboration with sponsors, research infrastructure teams, and ancillary departments to support the successful, ethical, and compliant conduct of clinical research.
Hourly range: $35.31-$56.82
Job Qualifications
Press space or enter keys to toggle section visibility
Required:
Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience.
Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.
Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.
Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.
Ability to respond to situations in an appropriate and professional manner.
Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
Ability to be flexible in handling work delegated by more than one individual.
Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.
Ability to handle confidential material information with judgement and discretion.
Working knowledge of the clinical research regulatory framework and institutional requirements.
Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.
Apply Now
Apply Now
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
Flexible Hybrid
Work Schedule
Monday-Friday 8am-5pm
Salary Range: $35.31 - 56.82 Hourly
Employment Type
2 - Staff: Career
Duration
Indefinite
Job #
28463
Primary Duties and Responsibilities
Press space or enter keys to toggle section visibility
The Department of Medicine is seeking a Clinical Research Coordinator to support the full lifecycle of clinical research studies, from study design and start-up through conduct and closeout. The incumbent will be responsible for implementing and coordinating research activities for one or more studies, managing day-to-day operations, and prioritizing tasks to ensure milestones and deadlines are met.
Working closely with the Principal Investigator and a wide range of internal and external partners, the Clinical Research Coordinator will ensure studies are conducted in compliance with institutional policies, FDA regulations, and ICH Good Clinical Practice (GCP). Responsibilities include study coordination, regulatory compliance, financial and operational oversight, and collaboration with sponsors, research infrastructure teams, and ancillary departments to support the successful, ethical, and compliant conduct of clinical research.
Hourly range: $35.31-$56.82
Job Qualifications
Press space or enter keys to toggle section visibility
Required:
Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience.
Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.
Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.
Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.
Ability to respond to situations in an appropriate and professional manner.
Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
Ability to be flexible in handling work delegated by more than one individual.
Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.
Ability to handle confidential material information with judgement and discretion.
Working knowledge of the clinical research regulatory framework and institutional requirements.
Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.
Apply Now
Apply Now