Contract Principal Investigator

Benefits

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

Responsibilities

• •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
• •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
• •10 more items(s)