We are seeking a Principal Investigator (PI) to lead and oversee clinical research studies while ensuring compliance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and the highest standards of patient safety and scientific integrity. This is an exciting opportunity to contribute to groundbreaking research that advances medical knowledge and improves patient outcomes.
Key Responsibilities
Serve as the Principal Investigator for clinical trials and research studies.
Ensure studies are conducted in compliance with study protocols, ICH-GCP guidelines, FDA regulations, and applicable local requirements.
Provide medical oversight and leadership throughout the research process.
Collaborate with sponsors, CROs, research coordinators, and site staff.
Review and approve study-related documentation, safety reports, and data.
Participate in monitoring visits, audits, and regulatory inspections.
Support patient recruitment, retention, and engagement initiatives.
Qualifications
Required
MD, DO, or equivalent medical degree with an active and unrestricted medical license.
Previous experience as a Principal Investigator or Sub-Investigator in clinical research preferred.
Knowledge of ICH-GCP, FDA regulations, and clinical trial processes.
Excellent leadership, organizational, and communication skills.
Board certification in a medical specialty preferred.
Tipo de puesto: Por contrato
Sueldo: $90,000.00 - $150,000.00 al año
Beneficios:
Lugar de trabajo: Empleo presencial
