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University leads major new research into wound care
17 September 2009
The University of York's Department of Health Sciences and NHS Leeds
Community Healthcare have been awarded a £1.75m grant from the National
Institute for Health Research to carry out a study into complex wounds.
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FDA panel backs Merck & Co sleep drug but at low doses
FDA panel backs Merck & Co sleep drug but at low doses
Boehringer in bother with FDA over manufacturing
Boehringer in bother with FDA over manufacturing
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Max Resourcing
Project Manager
Global Clinical Project Manager - home based
UK
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| Company: |
Torres And Partners |
| Category: |
Clinical Team Manager |
| Position: |
Clinical Research Manager |
| Area: |
UK |
| Location: |
North West |
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| Notes: |
Our client is a vibrant, exciting and fast-growing medical device company focused on the development and marketing of neurostimulation devices for the rehabilitation of stroke patients. Due to this growth, they now wish to appoint an experienced Clinical Research Associate/Manager who will ensure that their trials move forward positively, effectively and in line with national and international legislation.
Reporting to the Chief Operating Officer, the CRA/CRM will be responsible for working alongside external CROs and internally, with quality, scientific and clinical resources, to plan, monitor and report on clinical trials for product regulatory approval and post-market surveillance. This will require a close working relationship with the QA/RA Manager to ensure that all work is carried out to the latest applicable regulatory standards. Although primarily office-based, the CRM must be able to travel to conduct CRO and site audits, meet with regulatory bodies and attend other meetings as necessary. You’ll work alongside the external CRO in planning, implementing and monitoring international multi-site clinical trials.
Qualified to degree level in a relevant science subject or nursing, you’ll possess a minimum of 2 years CRA experience in medical device studies and possess a broad knowledge of the medical device environment, including MDD, AIMD and EN ISO 14155. You’ll also be able to demonstrate an understanding of ICH-GCP, global regulatory guidelines and the basics of clinical trial methodology. In addition, a full driving license is required.
Equally, you’ll have strong organisational, presentation and documentation skills, combined with the ability to work as part of a highly-focused team and also independently, taking responsibility for this area of company operations.
In return, you’ll receive competitive remuneration, share options and the opportunity to drive your career forward with a very exciting organisation.
Interested applicants are invited to Apply below or email a full CV, including current salary details to Torres and Partners at consultancy@torres.co.uk quoting reference CJM10147.
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| Reference: |
CJM10147
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| Contact: |
Kristin |
| Phone: |
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| Apply: |
Click Here
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