Company: Hobson Prior
Closing Date: 11 Nov 16
Salary (£): On Application
My client is a world leading Medical Device company who specialise in stents and grafts. They are seeking a Clinical Study Manager to join their team and be responsible for the development, set-up and maintenance of Clinical Trials.
Role: Clinical Study Manager
Role Type: Permanent, Full Time
My client is a world leading Medical Device company who specialise in stents and grafts.
They are seeking a Clinical Study Manager to join their team and be responsible for the development, set-up and maintenance of Clinical Trials.
Key responsibilities and duties will include but not limited to;
•Assist the Clinical Research Department with Clinical Trial activities
•Have input into specific Clinical Evaluation Reports
•Aid with regulatory submissions and ensuring compliance with relevant regulatory standards
• Prepare and submit clinical trial documentation to appropriate bodies
•Ensure the timely receipt, assessment and reporting of Adverse Events arising from Clinical Trials
•Ensure all medical devices issued during the course of a Clinical Trial are tracked in accordance with regulations and internal procedures.
•Supervise device distribution
•Responsible for pre-study visits, monitoring, close out visits
•Responsible for development of Clinical Investigation Plan and associated documentation
If you are interested in this position and would like to find out further details, please drop me over a copy of your CV to email@example.com or via our website.
Apply Here- applying is quick and easy on our new website
Hobson Prior International Ltd
7-9 Church Rd.
|Tel:||01892 612 612|
|Fax:||01892 612 613|
|Website:||Visit Our Web Site|
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