We are seeking a dedicated and detail-oriented Sub-Investigator to support the Principal Investigator in the conduct of clinical trials. The Sub-Investigator plays a key role in ensuring protocol compliance, patient safety, and data integrity throughout the study lifecycle.

• Assist the Principal Investigator in the overall conduct of clinical trials in accordance with the study protocol, ICH-GCP guidelines, and applicable regulations.
• Participate in subject recruitment, screening, informed consent, and clinical assessments.
• Document clinical findings accurately and timely in source documents and CRFs.
• Monitor and manage adverse events and report serious adverse events as required.
• Work closely with research staff to ensure proper study documentation and data quality.
• Attend investigator meetings, site initiation visits, and monitor visits as required.
• Maintain up-to-date knowledge of clinical trial protocols and amendments.
• Ensure the safety and wellbeing of study participants at all times.
  Pay: £31,189.00-£34,509.00 per year
  Work Location: In person
  Reference ID: SubInvestigato