Clinical Trials Assistant - Manchester, United Kingdom - The Christie NHS Foundation Trust

The Christie NHS Foundation Trust
The Christie NHS Foundation Trust
Verified Company
Manchester, United Kingdom

1 month ago

Tom O´Connor

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Tom O´Connor

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Description

Clinical Trials Assistant (Band 3) with scope to transition to a Clinical Trials Coordinator (Band 4) after a minimum 6-month competency review

We are offering a permanent contract for 37.5 hours per week for a Clinical Trials Assistant with growth potential to become a Clinical Trials Coordinator within the Rare Tumours research team at The Christie NHS Foundation Trust.

The research team belongs to the Research and Innovation division and is looking for an enthusiastic and experienced individual to assist with various aspects of clinical trial administration and coordination.

Applicants must meet all the essential criteria outlined in the job description.

  • Manage data and complete case report forms
  • Maintain site files and archives, handle invoicing
  • Communicate with trial sponsors, monitors, and the research community
  • Support the team and assist in setting up new studies

Effective communication and interpersonal skills are vital as you will interact with various staff members internally and externally.

The Christie, a leading cancer center in Europe, provides specialized cancer treatments to a large population and is renowned for its research breakthroughs.

They operate one of Europe's largest early clinical trial units with a strong reputation in cancer research.

DUTIES AND RESPONSIBILITIES

  • Act as a point of contact for research teams and sponsors
  • Assist in administrative tasks for trial set up
  • Maintain essential documentation and site files
  • Support safety reporting and data collection
  • Complete necessary team reporting mechanisms
  • Develop trial workbooks under supervision

Ensure the availability of clinical case notes and complete case report forms as required.

Liaise with NHS staff, handle confidential data, and arrange relevant trial-related meetings and document deliveries.

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