Senior Clinical Trials Coordinator

1 month ago

Northwood, Greater London, United Kingdom East and North Hertfordshire NHS Trust Full time
Job Overview

We are seeking a highly skilled and experienced Senior Clinical Trials Coordinator to join our Clinical Oncology Research Teams. As a key member of our team, you will play a vital role in supporting the clinical research team with all aspects of clinical trials administration, ensuring compliance with Good Clinical Practice (GCP), standard operating procedures (SOPs), and trust policies.

The successful candidate will have a strong understanding of the clinical trials process, including data management, and will be able to provide support to the Research Nurses and wider Clinical Research Team. You will also be responsible for supervising Band 4 Clinical Trial Coordinator(s) when required and overseeing the efficient and timely set up of clinical trials.

Main Duties
  • Support the clinical research team with all aspects of clinical trials administration, including data management.
  • Provide support to the Research Nurses and wider Clinical Research Team.
  • Supervise Band 4 Clinical Trial Coordinator(s) when required.
  • Oversee the efficient and timely set up of clinical trials.
  • Manage own workload for daily trial activity, including case report form completion and amendment processing.
Working for East and North Hertfordshire NHS Trust

We are a leading healthcare provider in the region, committed to delivering high-quality patient care and innovative research. Our values of Include, Respect, and Improve guide everything we do, and we are seeking a like-minded individual to join our team.

We offer a supportive and inclusive work environment, with opportunities for professional development and growth. Our staff are our greatest asset, and we are committed to supporting their well-being and work-life balance.

Person Specification

We are looking for a candidate with a degree-level education or equivalent experience, and relevant training courses in clinical research. Previous experience in clinical trial administration, including data management, is essential, as is experience of working in a healthcare setting and staff supervision/management.

The ideal candidate will have good organisational skills, good computer skills, and good oral and written communication skills. They will also have attention to detail, the ability to understand case report forms, and knowledge of the clinical trials process, including GCP guidelines/EU directives.

We are committed to equality, diversity, and inclusion, and welcome applications from all qualified candidates. We are proud to be a Disability Confident employer and offer a range of support for staff with disabilities.

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