Clinical Research Investigator
2 weeks ago
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.
**Key Responsibilities**:
- Assist the Principal Investigator in the overall conduct of clinical trials in accordance with the study protocol, ICH-GCP guidelines, and applicable regulations.
- 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: SubInvestigator
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