​Clinical Trial Administrator

Location United Kingdom
Discipline: Clinical Research
Job type: Permanent
Salary: £Salary: On application
Contact name: Grace Ticehurst

Contact email: grace.ticehurst@rbwconsulting.com
Contact phone: +441293584300
Job ref: 21418
Published: 2 days ago
Expiry date: 08 May 2021

Location: Cheshire UK

Flexible home working / Minimum of 3 days a week in the office

A fantastic opportunity has arisen for a Clinical Trial Administrator to assist the research teams by providing administrative support to clinical projects. This would be an ideal position for a candidate with prior experience working within clinical trials to work on studies in a supportive and progressive environment. In his role you will support to the clinical development/project teams and maintaining a range of clinical documentation. This position is based in Cheshire and is an opportunity to learn new things while growing with the company.

Responsibilities:

  • Support the clinical trial activities with regard to time, cost and quality and in accordance with SOPs, ICH-GCP guidelines and relevant regulations

  • Set up and maintain the documentation folders associated with product development and the Trial Master File (TMF) in compliance with ICH-GCP

  • Ensure the TMF index is kept up to date

  • Coordinate the collection of essential documents during site set-up

  • Assist in the development of processes and procedures in order to ensure that robust forecasting and scheduling of trials occurs

  • Set up trial specific meetings, taking minutes and tracking screening and enrolment across clinical sites

  • Track and process investigator site payments

  • Assist the project team with preparation and shipment of clinical trial documentation including: Investigator Site File, Pharmacy File, Investigator Brochure, Protocol and study manuals.

The ideal candidate must have:

  • University degree or an equivalent combination of education, training & experience

  • 12 months previous experience as a CTA.

  • Experience of using electronic TMF systems

  • Preferable experience of using the DIA reference model.

  • Prior experience in Clinical Research

  • Full working proficiency in English

This is one of many roles I am recruiting for within Clinical Research. If you are interested in more information about this role or to hear about other opportunities, please call Grace at RBW Consulting on 01293 584300 or email Grace.ticehurst@rbwconsulting.com

Salary: On application