Glen Burnie, Maryland
Gainesville, Georgia
Indianapolis, Indiana
Georgia
Baltimore, Maryland
Bel Air, Maryland
Harrisburg, Pennsylvania
Easton, Maryland
West Los Angeles, California
Posted: 09-Aug-24
Location: Los Angeles, California
Salary: Open
Categories:
Internal Number: 141102021
The Clinical Research Coordinator contributes to the overalloperational management of clinical research/trial/study activities from design,set up, conduct, through closeout. In this role, you will be responsible forthe implementation of research activities for one or more studies. Performnecessary tasks to manage projects and prioritizes work to meet necessarydeadlines. You will be responsible for planning and organizing necessary tasksto ensure adherence to the study protocol and applicable regulations, such asinstitutional policy and procedures, FDA Code of Federal Regulations (CFR), andICH Good Clinical Practice (GCP). The Clinical Research Coordinatorcollaborates with the Principal Investigator (PI), ancillary departments,central research infrastructure teams, sponsors, institutions, and otherentities as needed to support the administration of all aspects of studies,including, but not limited to, compliant conduct, financial management, andadequate personnel support.
Salary offers are determined based on various factors including,but not limited to, qualifications, experience, and equity. UCLA Health hourlysalary range for this position is $33.63- $54.11.
Required:
- Bachelor's degree or 1-3 years of previous study coordination orclinical research coordination experience.
- Strong verbal and written communication skills along with stronginterpersonal skills to effectively establish rapport, and build collaboraterelationships.
- Strong organizational capabilities to organize multiple projectsand competing deadlines for efficiency and cost-effectiveness.
- Analytical skills sufficient to work and solve address problemsand identify solutions with reasoned judgment.
- Ability to adapt to changing job demands and priorities; workflexible hours to accommodate research deadlines.
- Ability to be flexible in handling work delegated by more than oneindividual.
- Working knowledge of the clinical research regulatory frameworkand institutional requirements.
- Mathematical skills sufficient to prepare clinical researchbudgets, knowledge of math ability and knowledge of clinical trials researchbudgeting process to assist with the preparation of clinical trial budgets.
- Working knowledge of FDA Code of Federal Regulations (CFR) and ICHGood Clinical Practice (GC) for clinical research.
- Be available to work in more than one environment, travel tomeetings, off-site visits, conferences, etc.
