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  • Location: Dunfermline
  • Salary: £££ TBD on application plus bonus & benefits
  • Job Type:Permanent

Posted about 1 month ago

  • Sector: Clinical Operations
  • Contact: Alex Butcher
  • Contact Email:
  • Contact Phone: 01403 216216
  • Start Date: 2021-03-15
  • Job Ref: V-46575-1

An exciting opportunity arised for an experienced Clinical Data Manager to be the key member of the Clinical Data Management team to assist with product development and lead studies either inhouse or outsourced with a growing company in Dunfermline. Due to current restrictions, the position will be remote based with occasional visits to the Dunfermline office, if essential.

The Role
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 is offered complementing a friendly and supportive company environment and valued employee ethos.

A competitive salary is offered backed a generous benefits package which includes a bonus. The company believe their employees are their most valuable asset.

The successful candidate will need to have gained 3 -5 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.