Sub Investigator

Overview As a Sub-Investigator (Sub-I) , you will support the Principal Investigator (PI) in the safe and compliant conduct of clinical trials. You will take responsibility for delegated medical and trial-related activities, ensuring participant safety, high-quality data collection, and adherence to study protocols and regulatory requirements. Key Responsibilities Participant Screening & Medical Oversight Conduct medical assessments, including physical examinations, ECG interpretation, blood sampling, and spirometry. Confirm patient eligibility against trial criteria and support participant randomisation. Consent & Follow-up Obtain informed consent in line with ethical and Good Clinical Practice (GCP) standards. Carry out clinical follow-up visits, including assessments, investigations, and safety checks. Safety Monitoring & Reporting Monitor participants clinical status and review test results for safety concerns. Report adverse events, protocol deviations, and other safety issues to the PI in a timely manner. Regulatory Compliance & Documentation Maintain accurate and complete records in case report forms (CRFs) and electronic databases. Ensure all activities are conducted in accordance with protocol, GCP, and inspection standards. Team Collaboration Work closely with Research Nurses, Coordinators, and Data Managers to support smooth trial delivery. Attend site initiation visits, monitoring visits, and investigator meetings as required. Professional Development & Engagement Keep up to date with GCP training and relevant clinical research developments. Contribute to academic activities such as audit, quality improvement, and, where appropriate, publications. Essential Qualifications & Requirements Fully qualified medical doctor with current GMC registration. Up-to-date Good Clinical Practice (GCP) training. Experience in clinical research or clinical trial participation (desirable but not always essential). Competence in standard medical procedures such as venepuncture, ECG interpretation, and patient examination. Strong communication, organisational, and teamwork skills. Ability to work to protocols with high attention to detail. Desirable Attributes Experience working in a clinical research environment. Advanced Life Support (ALS) certification. Interest in academic research and contribution to publications. Benefits & Opportunities Opportunity to gain experience in early- and late-phase clinical trials. Exposure to a wide range of therapeutic areas and trial designs. Professional development in research methodology and trial leadership. Potential to contribute to publications, conference presentations, and further academic research.55b20050-bc17-4e5d-bfce-3c406318dffc

Created: 2025-09-04