Clinical Research Coordinator - Surgery
$36.37 - $58.52 per hourUniversity of California
Description
TheDepartment of Surgery is seeking an experienced Clinical Research Coordinatorto support interventional clinical trials across multiple divisions. This rolewill be responsible for coordinating and managing study activities for bothdrug and device trials, including participant recruitment, study implementation,data collection, and ensuring compliance with all regulatory requirements, institutionalpolicies, and study protocols.
Hourly Salary Range: $36.37 - $58.52
QualificationsRequired:
- BachelorsDegree or 1-3 years of previous study coordination or clinical researchcoordination experience
- Strong verbaland written communication skills along with strong interpersonal skills toeffectively establish rapport, and build collaborate relationships.
- Strong organizationalcapabilities to organize multiple projects and competing deadlines forefficiency and cost-effectiveness.
- Analyticalskills sufficient to work and solve address problems and identify solutionswith reasoned judgment.
- Ability toadapt to changing job demands and priorities; work flexible hours toaccommodate research deadlines.
- Ability torespond to situations in an appropriate and professional manner.
- Ability toconcentrate and focus in a work environment that contains distracting stimuliand competing deadlines.
- Ability to beflexible in handling work delegated by more than one individual. Al Required
- Typing andcomputer skill/ability including word-processing, use of spreadsheets, email,data entry. Ability to navigate numerous software programs andapplications.
- Ability tohandle confidential material information with judgement anddiscretion.
- Workingknowledge of the clinical research regulatory framework and institutionalrequirements.
- Mathematicalskills sufficient to prepare clinical research budgets, knowledge of mathability and knowledge of clinical trials research budgeting process to assistwith the preparation of clinical trial budgets.
- Workingknowledge of FDA Code of Federal Regulations (CFR) and ICH Good
- ClinicalPractice (GC) for clinical research.
- Be availableto work in more than one environment, travel to meetings, off-site visits,conferences, etc.
Required
Preferred
Job Industries
- Other
Vacancy posted 4 days ago
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