Job Search and Career Advice Platform

Enable job alerts via email!

Pediatric Clinical Trials Administrator & Data Specialist

The Royal Marsden NHS Foundation Trust

Greater London

On-site

GBP 30,000 - 40,000

Full time

7 days ago
Be an early applicant

Generate a tailored resume in minutes

Land an interview and earn more. Learn more

Job summary

A leading cancer research facility is seeking a Clinical Trials Administrator to support paediatric cancer research. Key responsibilities include ensuring high standards of data collection, managing trial documentation, and supporting the clinical research team. The ideal candidate is self-motivated, organized, and possesses excellent communication and IT skills. This role does not involve patient contact and is crucial for the efficient delivery of clinical trials as well as compliance with GCP standards.

Benefits

Learning and development opportunities
Flexible working arrangements
Stimulating and dynamic working environment

Qualifications

  • Previous NHS research experience within the paediatric setting is preferred.
  • Familiarity with Good Clinical Practice (GCP) and standard operating procedures.
  • Experience in clinical trial data collection and administration.

Responsibilities

  • Ensure data collection and (e)CRF completion meets required standards.
  • Design tools for clinical trial data capture.
  • Report on data entry status for analysis deadlines.
  • Represent Data Management at research meetings.

Skills

Excellent communication skills
Strong administrative skills
IT proficiency
Attention to detail
Ability to work independently
Job description
A leading cancer research facility is seeking a Clinical Trials Administrator to support paediatric cancer research. Key responsibilities include ensuring high standards of data collection, managing trial documentation, and supporting the clinical research team. The ideal candidate is self-motivated, organized, and possesses excellent communication and IT skills. This role does not involve patient contact and is crucial for the efficient delivery of clinical trials as well as compliance with GCP standards.
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.