Clinical Study Manager

Crewe, UK
23 May 2019
27 May 2019
Contract Type
Full Time
Clinical Study Manager
Crewe, Cheshire

Are you a talented clinical professional, with experience in the medical arena? Are you skilled at planning, coordinating and executing clinical projects? If so, read on.

The Company

Based in the UK since 1999, Medtrade is an independent company with a legacy of developing technologically advanced solutions in woundcare, trauma woundcare and surgical woundcare. We are the innovator, developer and manufacturer of the Celox product range. Due to expansion and growth of the business, Medtrade are now looking for a Clinical Study Manager to join our team in Crewe.

The Benefits

- Competitive salary
- Contributory pension scheme
- Life assurance
- 25 days' holiday plus public holidays
- 37.5 hour week

The Role

As a Clinical Study Manager, you will have a leading role in the overall management of Medtrade's clinical strategy. You will be a key player in the provision of clinical advice and guidance to the NPD and design change teams, ensuring compliance with applicable regulations.

In addition, you will:

- Write and maintain clinical evaluation reports to meet the requirements of the EU Medical Device Regulation
- Establish and maintain procedures to ensure adherence to trial protocols and administrative requirements
- Manage post-market surveillance/post market clinical follow up activities for existing and new devices
- Create and maintain all trial files, including the trial master file, and oversight of site files
- Write clinical trial notifications and investigational device exemptions for submission to regulatory bodies
- Manage the overall efficient day-to-day management of the trials through third party clinical trial organisations

This is an important role with far-reaching impact that will afford the successful candidate an exciting career and continuous opportunities for growth.

About You

To be considered, you'll need:

- A bachelor's degree, or equivalent, in business management, biology, health care management, or a related field
- Previous experience as a clinical study manager
- A full, UK driving licence (you will be travelling around 25% of the time)
- Demonstrable skills and aptitude for leading on projects
- Excellent communication skills that enable you to translate complex findings and data into digestible presentations, literature.etc.

A post bachelor's degree certificate, or equivalent, for clinical trial manager (including advanced training in clinical research writing, site management, and statistical analysis) would be advantageous to your application.

Our client is eager to hear from candidates who have worked as a Clinical Case Manager, Clinical Project Manager, Study Manager, Clinical Trial Manager, Clinical Trial Coordinator, or Clinical Trials Programme Manager.

Webrecruit and Medtrade are equal opportunities employers, value diversity and are strongly committed to providing equal employment opportunities for all employees and all applicants for employment. Equal opportunities are the only acceptable way to conduct business and we believe that the more inclusive our environments are, the better our work will be.

So, if you're a talented Clinical Study Manager, please apply via the button shown. This vacancy is being advertised by Webrecruit. The services advertised by Webrecruit are those of an Employment Agency.

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