UCLA Health
Study Coordinator, Neurology
UCLA Health, Los Angeles, California, United States, 90079
Description
The Study Coordinator contributes to the overall operational
management of clinical research/trial/study activities from design, set up,
conduct, through closeout. You will be responsible for the implementation of
research activities for one or more studies. The Study Coordinator recognizes
and performs necessary tasks to manage projects and prioritizes work to meet
necessary deadlines. You are responsible for planning and organizing necessary
tasks to ensure adherence to the study protocol and applicable regulations,
such as institutional policy and procedures, FDA Code of Federal Regulations
(CFR), and ICH Good Clinical Practice (GCP). You will collaborate with the
Principal Investigator (PI), ancillary departments, central research
infrastructure teams, sponsors, institutions, and other entities as needed to
support the administration of all aspects of studies, including, but not
limited to compliant conduct, financial management, and adequate personnel
support.
Salary Range: $33.63 - $54.11/Hourly
Qualifications
All 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 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 with judgement and discretion.
Working knowledge of the clinical research regulatory framework and institutional requirements.
Mathematical skills sufficient to prepare clinical research budgets.
Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
Available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.
UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.
The Study Coordinator contributes to the overall operational
management of clinical research/trial/study activities from design, set up,
conduct, through closeout. You will be responsible for the implementation of
research activities for one or more studies. The Study Coordinator recognizes
and performs necessary tasks to manage projects and prioritizes work to meet
necessary deadlines. You are responsible for planning and organizing necessary
tasks to ensure adherence to the study protocol and applicable regulations,
such as institutional policy and procedures, FDA Code of Federal Regulations
(CFR), and ICH Good Clinical Practice (GCP). You will collaborate with the
Principal Investigator (PI), ancillary departments, central research
infrastructure teams, sponsors, institutions, and other entities as needed to
support the administration of all aspects of studies, including, but not
limited to compliant conduct, financial management, and adequate personnel
support.
Salary Range: $33.63 - $54.11/Hourly
Qualifications
All 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 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 with judgement and discretion.
Working knowledge of the clinical research regulatory framework and institutional requirements.
Mathematical skills sufficient to prepare clinical research budgets.
Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
Available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.
UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.