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Clinical Trials Coordinator | The Royal Marsden NHS Foundation Trust

The Royal Marsden NHS Foundation Trust

London

On-site

GBP 30,000 - 45,000

Full time

2 days ago
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Job summary

A leading healthcare organization in London is seeking a Clinical Trial Coordinator to manage and oversee clinical trials in the Lung Research Team. This role offers an excellent opportunity for professional growth in a prestigious cancer center known for research and patient care. Candidates should have experience in clinical trial management and knowledge of Good Clinical Practice standards. Flexibility and dedication to excellence are key attributes for this role.

Benefits

Opportunities for professional development
Flexible working options
Wide range of staff benefits

Qualifications

  • Experience in coordinating clinical trials.
  • Knowledge of Good Clinical Practice guidelines.
  • Ability to manage multiple trials in a clinical setting.

Responsibilities

  • Coordinate and oversee clinical trials day-to-day.
  • Ensure trials comply with sponsor and regulatory requirements.
  • Report on activity within the department and highlight concerns.

Skills

Clinical trial management
Regulatory compliance
Good Clinical Practice (GCP)
Team collaboration

Job description


Clinical Trial Coordinator, Lung and Mesothelioma Research.
The Royal Marsden NHS Foundation Trust has an international reputation for high quality patient care, education and research and its partnership with The Institute of Cancer Research (ICR) has created the largest comprehensive cancer centre in Europe.

This role is based within the Lung Research Team at The Royal Marsden (located at two sites – Sutton, Surrey and Chelsea, London), which is world renowned for excellence in clinical care and clinical research.
Applications are invited for a Clinical Trial Coordinator role which is a 12 month fixed-term post, with possibility of extension.

For further details contact: Bianca.Rock@rmh.nhs.uk
• Responsible for the day-to-day coordination and oversight of allocated clinical trials in the Department.
• Responsible for the set-up and conduct of allocated clinical trials in accordance with regulatory, sponsor and organisational requirements.
• Ensure clinical trials within the Unit are conducted in accordance with Good Clinical Practice and Trust SOPs.
• Review the capacity and resource requirements within the Clinical unit for coordination and administrative management of the allocated trials and to advise the unit head accordingly.
• To be an active member of the department, providing regular reports on activity within the Department and highlighting areas of concern.

The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals – one in Chelsea, London, and one in Sutton, Surrey – as well as a Medical Daycare Unit in Kingston Hospital.

At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.

At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways. There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance. We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements.

For further information on this role, please see the attached detailed Job Description and Person Specification:
• To be responsible for maintaining own professional development and be aware of current practices and future developments within the Trust and National Health Service.
• To aid in the implementation of corrective and preventative measures within the Unit as agreed with the Unit Head.
• To support the Clinical R&D Office in preparation for regulatory inspections.
• To take an active role in the Unit and the Trust as a member of a clinical research team.
• To help coordinate the Unit’s research meeting ensuring appropriate, documented monitoring of the clinical trial portfolio.


This advert closes on Monday 28 Jul 2025
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