Physician Sub-Investigator Consultant
Core
Medical oversight of clinical trial participants including screening, dosing supervision, and adverse event management.
Role type
Physician Sub-Investigator Consultant
Builds
Clinical trial data and patient safety records for pharmaceutical/biotech sponsors
Domain
Clinical Research / Biopharmaceuticals
Deliverable
client delivery
Required skills
ABIM board certification in internal medicine, active Florida medical license, DEA registration, GCP/ICH guidelines knowledge, ECG interpretation, lab review, adverse event management, protocol compliance
Preferred skills
Subspecialization in internal medicine, experience with Investigator 1572 Form
Technologies
ECG machines, laboratory analyzers, electronic source documents
Responsibilities
Perform physical examinations and eligibility assessments for study participants, supervise investigational product dosing, interpret ECGs and review lab results, manage and report adverse events, approve subject admission and randomization, document findings in source documents, provide medical management for adverse events, communicate with sponsors and auditors, monitor participant safety, provide coverage for the Clinic Principal Investigator
Seniority
Senior, hands-on IC