As a Clinical Investigator, you will be responsible for overseeing the design, conduct, and documentation of clinical trials, ensuring they adhere to study protocols and regulatory requirements. This includes recruiting and monitoring participants, managing informed consent, interpreting results, and maintaining high-quality study records. You will work closely with research coordinators, regulatory agencies, sponsors, and other healthcare professionals to support the integrity and progress of clinical research. Ensuring patient safety and compliance throughout the process is also a key part of your daily work. This role offers a dynamic environment with opportunities to develop expertise in clinical research methodologies and regulatory affairs.