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Contract Principal Investigator at Circuit Clinical

Middletown, New York, United States -

Full Time

Start Date

Immediate

Expiry Date

12 May, 26

Salary

0.0

Posted On

11 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Regulatory Compliance, Patient Safety, Protocol Compliance, Medical Oversight, Adverse Event Review, Patient Eligibility, Study Assessments, Informed Consent, Monitoring Visits, GCP Training, Study Team Meetings, Webinars, PI Meetings, Vaccine Trials, FDA Regulations

Industry

Research Services

Description

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.

Responsibilities

The Contract Principal Investigator will oversee the feasibility, start-up, maintenance, and closeout of clinical research projects. Responsibilities include ensuring subject safety, protocol compliance, and providing medical oversight throughout the study.