Looking for a strong Clinical Research Coordinator with 3+ years of experience for a Study Coordinator contract position.
Where : ONSITE in San Diego, California - NO option for remote flexibility
Duration : 4-6 month contract, possibility of extension
Therapeutic Area : Ophthalmology - experience with this indication is not required
Responsibilities :
- Chart review
- Data entry and data migration
- Assist with study visits
- Sample collection and processing - excluding venipuncture and study drug administration
- Pre-screening for eligibility to protocol
- Query resolution
- Audit preparation monitoring visits
- AE monitoring
- Consenting
- Scheduling and appointment reminders
- Source document creation
- Administrative tasks maintaining study binder, regulatory filing, etc.
- Regulatory document maintenance, preparation, and submission of study level IRB / Regulatory documents from approved templates
Clinical Research Coordinator
Nursing, Biology, Public Health)Minimum of 1 year of experience in clinical researchKnowledge of Good Clinical Practice (GCP), FDA regulations, and IRB processesExperience with electronic medical records (EMR) systems is a plusCertification in clinical research (e. A company is looking for a Clinica...
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