What are the responsibilities and job description for the Contract Principal Investigator position at Circuit Clinical?
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 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.
Salary : $120 - $150