Clinical Trials Project Coordinator - Maids Moreton, United Kingdom - Vitalograph

Vitalograph
Vitalograph
Verified Company
Maids Moreton, United Kingdom

3 weeks ago

Tom O´Connor

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Tom O´Connor

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Description

Clinical Trials Project Coordinator - Vitalograph

Hybrid (Maids Moreton, Buckingham, UK)

Benefits:


  • Company contributed pension
  • Private Health Insurance
  • Educational assistance programme
  • Development & progression opportunities
  • Subsidised local accommodation available
Salary from £25,000.00 per annum


About Us


Vitalograph is a leading manufacturer of medical respiratory diagnostic devices and software, used in the diagnosis of respiratory disorders, and advanced high-reliability equipment and software systems used in respiratory end-point clinical drug trials.

We have designed and manufactured respiratory diagnostic devices, software, and consumables for healthcare professionals, for almost 60 years and serve customers in over 100 countries.

Headquartered in the UK, Vitalograph has operations in Ireland, Germany and the USA.

We have an exciting opportunity to join our Clinical Trials Team as a Project Coordinator on a permanent contract.

The Project Coordinator will provide an excellent service to Vitalograph customers by supporting the delivery of clinical trials services across multiple projects and reporting on those services.


Roles & Responsibilities:


  • Assisting Project Managers with general study duties
  • Assist in monitoring for GCP compliance within centralized clinical trials
  • Assist with reporting on study progress
  • Assist with problem solving project issues
  • Assist with training Monitors and Investigators
  • Writing study related documents as requested by Project Team
  • Assist with writing, updating and organising translation and printing of study manuals
  • Ensuring any study related documents are filed and stored appropriately

Skills and Experience:


Essential:

  • An excellent attention to detail in work carried out.
  • Good organisation skills; being able to effectively plan and carryout tasks within the required timeframe.
  • Customer service experience and able to demonstrate effective communication and interpersonal skills
  • Problem solving in the work environment
  • Excellent written English
  • Strong IT skills e.g. MS Word, Excel and PowerPoint.

Desirable:

  • Awareness of GCP and Clinical Trials terminology
  • Experience of working to SOP
  • Experience of working in Clinical Trials
  • Bioscience graduate
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