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 reports for pharmaceutical/biotech sponsors
Domain
Clinical Research / Pharmacology
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, eligibility assessment, adverse event management, protocol compliance
Preferred skills
Subspecialization in internal medicine, experience in hospital or clinic-based practices
Technologies
ECG machines, laboratory analyzers, electronic source documentation systems
Responsibilities
Perform physical examinations and eligibility assessments for study participants, supervise investigational product dosing, interpret ECGs and review lab results, manage and document adverse events, approve subject admission and randomization, communicate with sponsors and auditors, provide coverage for the Clinic Principal Investigator
Seniority
Mid-level, hands-on IC
