Principal Investigator (Hybrid)

Job Description

Overview

The Principal Investigator is the physician responsible for the medical leadership, safety, and successful delivery of clinical trials at a research site. They ensure every study is conducted ethically, in line with regulatory standards, and with participant wellbeing at the Centre.

Key Responsibilities

• Provide overall medical oversight for trials and ensure studies follow GCP.
• Protect participant safety, rights, and confidentiality.
• Review protocols, evaluate medical history, and conduct trial-related assessments.
• Interpret clinical data, lab results, ECGs, and diagnostics.
• Report Serious Adverse Events (SAEs) on time.
• Oversee administration of investigational products.
• Keep accurate documentation and ensure compliance with ethics/regulatory boards.
• Support feasibility checks and answer sponsor queries.
• Participate in audits, monitoring visits, and inspections.

• Skills & Competencies

  • Strong knowledge of ICH GCP and clinical research ethics.
  • Excellent clinical judgment and attention to detail.
  • Clear communicator and effective collaborator.
  • Analytical problem-solver with flexibility.

  
  

  Qualifications

  • MD or DO with an active medical license (valid where the research is conducted).
  • Board certified/board eligible in a relevant specialty.
  • GCP certified.
  • Previous clinical research experience .
  • Willing to complete training and follow company SOPs.