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Palo Alto, CA
3 months ago
Clinical Research Coordinator
This is a contract position and requires previous Ophthalmology clinical research experience
Job Description:
Looking to hire an onsite full 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:
- Patient recruitment
- Chart review of patient medical records
- Phone screening
- Informed consent
- Collection of study data and entering into EDC
- Resolving queries
- Medical record retrieval
- Creating source documents
- E-diary compliance
- IRB approval
- Assist with timely reporting of AEs/SAEs
- Maintaining study binders
- Specimen collection and processing
- Subject follow-up
Qualifications:
- Minimum of two years in a Clinical Research Coordinator role
- Ophthalmology experience required
- Experience with electronic medical records (EMR)
- Experience with electronic data capture (EDC) systems
Additional Details:
Location: Palo Alto, CA
Duration: Contract until December 2024 with possible extension
Schedule: Onsite 40 hours/week (Monday-Friday) - during normal business hours
Hourly pay range: $30-45 per hour
Start Date: ASA
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