Clinical Research Coordinator
*Role will start at part time hours*
Job Description:
Looking to hire an onsite part time individual with clinical research experience to act as a consultant CRC to support an ongoing Ophthalmology clinical trial. This CRC must be experienced in being able to work independently. You will act as one of the main CRC’s for this study. Please note, as the position and study progress, additional job duties will likely be added that are not listed in this description. A candidate must help the site and study wherever needed depending on the specific assignment.
Responsibilities:
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Chart review
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Pre-screening for eligibility
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Informed consent
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Data entry
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Data migration
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Query resolution
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AE/SAEs
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Source document storage
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Study visit preparation
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Assist with study visits
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Sample collection and processing
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Regulatory document maintenance
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IRB submissions
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Scheduling appointments and reminders
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Any study efforts deemed necessary by the site
Qualifications:
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Minimum of two years in a Clinical Research Coordinator role
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Ophthalmology clinical trial experience preferred
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Regulatory experience required
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Experience with electronic medical records (EMR)
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Experience with electronic data capture (EDC) systems
Additional Details:
Location: Los Angeles, CA - zip code 90033
Duration: 9 month contract with possible extension
Schedule: Will start at 20 hours, potential for it to go to full time hours - during normal business hours
Hourly pay range: $30-40 per hour
Start date: ASAP
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