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Clinical Data Manager

Clinical Data Manager

Job Title: Clinical Data Manager
Contract Type: Permanent
Location: Dunfermline
Industry:
Salary: Up to £35,000
Start Date: ASAP
Reference: 15833 JM
Contact Name: Julie McEwan
Contact Email: julie.mcewan@nextphaserecruitment.com
Job Published: April 17, 2018 12:55

Job Description

The Role

My client based in Dunfermline, have an opportunity for an experienced Clinical Data Manager to join their team. You will be responsible for the development of clinical database and all study documentation, including maintenance of the Trial Master File. As an integral part of the team you will provide support to the Clinical Data Management Director with respect to User Acceptance Testing scripts and training for all users regarding Electronic Data Capture and continual review of the company’s Data Management Plan and Data Handling Manual to ensure regulatory compliance.

The Company

A growing medical device company, operating on a global platform that specialises in the diagnosis, treatment and prevention of retinal diseases and disorders. With over 25 years’ experience within this sector to draw upon they are at the forefront of innovation.  Placing high importance on work/life balance the company believe that professional and personal goals are of equal importance and provide an environment where both can be realised. A competitive salary and extensive benefits package are offered complementing a friendly and supportive company environment and valued employee ethos.

Benefits

A competitive salary is offered backed by an extensive benefits package including 34 days annual leave (including bank holidays), company bonus, contributory pension, flexi-time, private health care and insurance schemes.  The company believe their employees are their most valuable asset.

Experience

The successful candidate will need to have gained at least four years clinical data management experience gained within medical devices or pharmaceuticals and be able to demonstrate an excellent understanding of Good Clinical Practice and Good Manufacturing Practice. A strong understanding of the clinical trial process and the accompanying regulatory requirements is also essential; alongside a key attention to detail and a highly organised nature. Prior working knowledge of clinical database, electronic data capture and clinical trial management systems is imperative.