Traveling Sub-Investigator (MD/DO) - Clinical Research, Multi State License
Job at a glance
Job description
The Traveling Sub-Investigator (SI) provides medical oversight & clinical support for participants enrolled in a clinical research study for patients aged 2-65. This role is responsible for patient safety, protocol compliance, investigational product oversight, and timely clinical documentation throughout all phases of the study.
The ideal candidate is comfortable working in a fast-paced, evolving clinical research environment & demonstrates adaptability, accountability, responsiveness and strong clinical judgment while supporting medically complex pediatric participants and their families.
This position requires frequent travel to participant homes, clinical sites and study-related locations to support decentralized and home-based clinical trial activities.
Job Responsibilities
* Conduct & oversee protocol-required assessments including physical examinations, neurological evaluations, safety assessments & study procedures.
* Monitor participant safety throughout the study, including adverse events, lab abnormalities & other significant clinical findings.
* Respond promptly and appropriately to participant safety concerns, protocol deviations, medical escalations, and urgent study-related issues.
* Make medical decisions regarding investigational product continuation, interruption, dose adjustment, or discontinuation in accordance with protocol and participant safety requirements.
* Support medically complex pediatric participants in both clinical and home based research settings.
Additional details and engagement requirements to be discussed in pre-screening.
Qualifications
Working Hours
Florida New Jersey Connecticut Pennsylvania
Georgia New Hampshire Vermont New York
Michigan Rhode Island Colorado Idaho
Nevada North Carolina South Carolina Tennessee
Alabama Arkansas Louisiana Maryland
Virginia West Virginia California Washington