Principal Investigator

Principal Investigator

Overview

We're looking for an experienced Principal Investigator to lead the delivery of clinical trials while ensuring the highest standards of patient safety, regulatory compliance, and data integrity. You'll work closely with sponsors, CROs, and research teams to drive successful study outcomes.

Key Responsibilities

• Lead Phase I–IV clinical trials.
• Ensure compliance with ICH-GCP and regulatory requirements.
• Protect participant safety and oversee informed consent.
• Assess patient eligibility and perform study-related clinical evaluations.
• Review and report AEs/SAEs.
• Maintain accurate study documentation and data quality.
• Collaborate with sponsors, CROs, and regulatory bodies.
• Support monitoring visits, audits, and inspections.
• Lead and mentor site research staff.

Requirements

• MD, DO, MBBS, or equivalent.
• Previous Principal Investigator or Sub-Investigator experience.
• Strong knowledge of ICH-GCP and clinical research regulations.
• Excellent leadership and communication skills.
• Ability to manage multiple clinical studies in a fast-paced environment.

If you're passionate about advancing clinical research and improving patient outcomes, we'd love to hear from you.