Clinical Research Coordinator job at reputed company in Los Angeles, CA
Title: Clinical Research Coordinator
Location: Los Angeles reputed company
Job reputed company:
General Information
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Work Location: Los Angeles, CA, USA
Onsite or Remote
Flexible Hybrid
Work Schedule
Monday-Friday reputed company-5pm
Salary reputed company: $35.31 - 56.82 reputed company
Employment Type
2 - Staff: Career
Duration
Indefinite
Job #
28463
Primary Duties and Responsibilities
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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 reputed company Investigator and a wide reputed company of reputed company partners, the Clinical Research Coordinator will ensure studies are conducted in compliance with institutional policies, FDA regulations, and ICH Good Clinical reputed company (GCP). Responsibilities include study coordination, regulatory compliance, financial and operational reputed company, and collaboration with sponsors, research infrastructure teams, and ancillary departments to support the successful, ethical, and compliant conduct of clinical research.
reputed company reputed company: $35.31-$56.82
Job Qualifications
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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 reputed company and competing deadlines for efficiency and cost-effectiveness.
Analytical skills sufficient to work and solve address problems and reputed company with reasoned judgment.
Ability to adapt to changing job demands and priorities; work reputed company to accommodate research deadlines.
Ability to respond to situations in an appropriate and reputed company manner.
Ability to concentrate and reputed company 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 reputed company/ability including word-processing, use of spreadsheets, email, data entry. Ability to reputed company numerous software programs and applications.
Ability to handle confidential material information with judgement and discretion.
Working knowledge of the clinical research regulatory reputed company and institutional requirements.
Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of reputed company research budgeting process to assist with the preparation of clinical trial budgets.
Working knowledge of FDA reputed company of Federal Regulations (CFR) and ICH Good Clinical reputed company (GC) for clinical research.
Be available to work in more than one environment, travel to meetings, off-site reputed company, conferences, etc.
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