Oncology Principal Investigator l Part-Time (1099) l 243430

As a Principal Investigator, you will provide medical oversight and leadership for oncology clinical trials. You will be responsible for ensuring subject safety, regulatory compliance, and protocol adherence throughout the duration of the study. Our site team will support you with daily operations, allowing you to focus on medical decision-making and oversight. Key Responsibilities: Serve as Principal Investigator on assigned oncology clinical trials Conduct and/or oversee study-related assessments, including subject eligibility, informed consent and safety evaluations Ensure compliance with study protocols, GCP, FDA regulations, and IRB requirements Collaborate with study sponsors, CROs, and internal staff throughout the trial lifecycle Review and sign off on case report forms (CRFs), adverse events, and safety data Participate in Site Initiation Visits, Monitoring Visits, Investigator Meetings and other Sponsor meetings as needed Provide guidance and medical support to the research team