Trial Manager / Clinical Research Practitioner II

Guy's and St Thomas' NHS Foundation Trust; London; On-site; GBP 30,000 - 42,000; Part time

Job summary

Join a prestigious NHS Trust as a Clinical Research Practitioner managing the LISA study, evaluating treatments for bacterial vaginosis and candida. This part-time role involves overseeing trial activities, participant recruitment, and data management across key research sites, ensuring adherence to quality standards.

Qualifications

• Experience in managing clinical trials and adherence to ICH-GCP standards.
• Strong communication skills to liaise with various stakeholders.

Responsibilities

• Manage day-to-day operations of the LISA trial and participant follow-up.
• Conduct qualitative interviews to support the study.
• Organise Trial Management and Steering Group meetings.

Skills

Research Management

Data Quality Control

Participant Follow-up

Qualitative Interviewing

Clinical Trials Coordination

Job description

We are seeking a dynamic and experienced Clinical Research Practitioner to manage the LISA study, a clinical trial investigating treatments for bacterial vaginosis and candida. This exciting study compares standard oral treatments to vaginal lactoferrin and includes both quantitative and qualitative components. The successful candidate will lead on all trial management activities including recruitment, data quality, participant follow-up, and sample handling, ensuring adherence to ICH-GCP standards.

This is a part-time position based across two main research sites: Burrell St Sexual Health Clinic and Curran General Practice in Clapham.

• Manage day-to-day operations of the LISA trial including recruitment, randomisation, consent, and follow-up of study participants.
• Conduct qualitative interviews with participants to support the study's mixed-methods design.
• Organise and lead Trial Management Group and Trial Steering Group meetings, presenting progress and recruitment updates.
• Liaise with Clinical Trials Unit to manage study database and randomisation system.
• Coordinate collaboration with internal departments (e.g., R&D, Pharmacy, Labs) and external bodies (e.g., IMP manufacturers).
• Develop and maintain trial-specific documentation, SOPs, and the Trial Master File (TMF).
• Organise and ensure quality control of participant sample packs and sample tracking, analysis, and storage.
• Support protocol amendment processes and represent the trial at conferences and stakeholder meetings.
  
  

You will be joining one of the UK’s most respected NHS Trusts, committed to delivering cutting-edge research that directly informs and enhances patient care. The Trust is a major centre for academic and clinical excellence and provides an inclusive, supportive environment for career development and research delivery.

For further details / informal visits contact: Name: Amy Day Job title: Research Manager Email address: [e-mail]

Due to volume of applications, your query may only be responded to if you are shortlisted for interview.