Clinical Research Investigator (Doctor) Part‑time opportunity – 2 days per week. We are looking for a dynamic doctor to join our established clinical research site in Miranda, NSW. Responsibilities Conduct studies in accordance with ICH GCP guidelines and ensure participant privacy and confidentiality per HIPAA and institutional regulations. Ensure study subjects’ rights, safety and well‑being. Participate in all study related meetings with CRO/Sponsor, including investigator meetings, pre‑selection visits, site initiation visits, monitoring visits and close‑out meetings. Understand study protocol, investigator’s brochure and informed consent form (ICF). Assess participant eligibility in accordance with protocols. Obtain informed consent prior to any study activities. Maintain clinical oversight of medical care, procedures and decisions regarding the study. Ensure the trial is conducted in compliance with the protocol and IRB/IEC approval. Assist with other trial roles when required (e.g., phlebotomy, ECGs, nasal swabs). Assist in efficient running and improvement of the clinical function. Oversee training log, delegation log and study‑specific training of all staff on trial. Maintain adequate records (Investigator Site File) of each subject’s participation, including investigations, adverse events, safety reports, protocol deviations and final reporting. Meet regularly with study‑assigned CRA to assess progress and performance. Compliance Accountabilities Ensure data quality and highest data quality standards. Make reasonable efforts to retain participants on the clinical trial. Ensure informed consent is adequately obtained for study subjects. Required Qualifications Bachelor of Medicine/Bachelor of Surgery or Medical Doctorate. General registration (Post‑graduate year 3 and above). Qualified by training, education and experience in clinical research. ICH‑GCP certificate (can be obtained on the job). Required Skills Superior analytical thinking skill. Excellent attention to detail and ability to keep detailed, accurate medical records. Up‑to‑date training with anaphylaxis/cardiac arrest management. ECG and other diagnostic procedures experience. Clinical research experience and clinical acumen. Proficiency in use of electronic medical record software. #J-18808-Ljbffr