Contract Principal Investigator

Description 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

• Serve as PI for industry sponsored clinical research trials Maintain ultimate regulatory responsibility for study conduct, subject safety, and protocol compliance Appropriately delegate study related activities to qualified research staff while providing ongoing oversite according to FDA regulations, local regulations, and ICH/GCP guidelines Provide medical oversight Review Adverse Events and Serious Adverse Events Confirm patient eligibility as defined in the research protocol Complete study assessments as required (i.e. physical exam) Participate in the consenting process and patient’s clinical research education Attend monitoring visits (Pre-study, Initiation, Interim and Close Out) on assigned studies Complete GCP/HSP, study specific, and system specific training per protocol and Circuit Clinical IT guidelines Participate in relevant study team meetings both internal and with the sponsor/CRO
• Participate in webinars and
• PI meetings as needed
• Your
• Qualifications: MD or DO License is required A Medical License in good standing in NY At least 1 year of experience working in clinical research. 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.