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 5 years’ 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.