Contract Principal Investigator

Contract Principal Investigator

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.