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.
Youll 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 patients 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.
Required Experience:
Staff IC
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 ma...
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.
Youll 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 patients 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.
Required Experience:
Staff IC
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