Circuit Clinical® is on a mission to transform the way people find, choose, and participate in clinical research.
We are searching for a Contract Principal Investigator.
This position is ultimately responsible for research project feasibility, research project start-up, screening visits, research project maintenance and follow up, research project closeout, and post-closeout safety follow-up.
You’ll Be Responsible For:
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Serve as PI for industry sponsored clinical research trials
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Maintain ultimate regulatory responsibility for study conduct, subject safety, and protocol compliance
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Appropriately delegate study related activities to qualified research staff while providing ongoing oversite according to FDA regulations, local regulations, and ICH/GCP guidelines
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Provide medical oversight
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Review Adverse Events and Serious Adverse Events
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Confirm patient eligibility as defined in the research protocol
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Complete study assessments as required (i.e. physical exam)
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Participate in the consenting process and patient’s clinical research education
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Attend monitoring visits (Pre-study, Initiation, Interim and Close Out) on assigned studies
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Complete GCP/HSP, study specific, and system specific training per protocol and Circuit Clinical IT guidelines
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Participate in relevant study team meetings both internal and with the sponsor/CRO
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Participate in webinars and PI meetings as needed
Your Qualifications:
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MD or DO License is required
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A Medical License in good standing in NY
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At least 1 year of experience working in clinical research.
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Experience in vaccine clinical trials preferred.
The fine print:
Location: This position is an on-site position working in our Middletown, New York site.
Employment: This is an independent contractor position working 15-20 hours per week, which could develop to 40 hours per week.
