Sub Investigator in North East Lincolnshire

Job description

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.

Extra information

Status

Open

Education Level

Secondary School

Location

North East Lincolnshire

Type of Contract

Part-time jobs

Published at

11-09-2025

Full UK/EU driving license preferred

No

Car Preferred

No

Must be eligible to work in the EU

No

Cover Letter Required

No

Languages

English