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Job titlePost Market Clinical Development Specialist
Job typeMeditech
Salary GBP
Bonus Package
Job description

A market-leading developer of single use instruments is currently looking for a Post Market Clinical Development Specialist to join their team in Denmark to be involved in new product development projects. If you are an experienced doctor who has moved into clinical research or trial management and are passionate about bringing products to market, this could be the perfect role for you. 

The company 

Our client has over 80 years’ of experience and a world-leading reputation in the single-use instruments space, with a focus on high-quality, cost-effective products that improve patient safety. They are rapidly growing and have strong projections for the future and are constantly making investments in new product development. Millions of patients and healthcare professionals worldwide depend on the functionality and performance of our client’s products.


The role 

As Post Market Clinical Development Specialist, you will play an important role in the Clinical Research team and will be responsible for the strategic direction that brings new products to market and supports market penetration. Our client aims to get their products to market quickly, without this impacting on quality and you will play a significant role in this by preparing the clinical documentation to support product approval. 

Responsibilities include: 

  • Preparing and advising on the contents of clinical documentation to support product approval 

  • Planning and reporting pre-clinical and clinical investigations 

  • Staying up to date in relevant clinical areas, including new regulations 

  • Planning and executing clinical evaluation of products and reviewing clinical documents 

  • Supporting other clinical staff in writing and documentation 

  • Helping to bring new products to market quickly and effectively, in line with clinical and quality regulations 

  • Driving continuous improvement and act as a champion for change  


The requirements 

You’ll be an experienced doctor within the anesthesia, intensive care or surgical sector, as well as… 

  • Degree educated in a relevant clinical discipline 

  • Knowledgeable in EU and FDA regulations and guidelines 

  • Clinical competence for medical device development projects 

  • Able to take ownership of projects and work collaboratively on projects 

  • Strong written and verbal English communication skills 

  • Able to make accurate judgements and decisions  

  • Experience driving continuous improvement initiatives 

  • A strategic thinker, analytical, and hyper-organised

  • You will ideally live in the Greater Copenhagen area or within a commutable distance to it


Important information 

FMC contact for the role: Charlotte Ashton ( 

Reference number: 11370 

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    Updated on 2017-08-07T17:04:38+00:00, by Matthew Graham.