Job Title

OverviewThe 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 ResponsibilitiesProvide 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 & CompetenciesStrong 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.QualificationsMD 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 preferred.Willing to complete training and follow company SOPs.