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Job titleSenior Post Market Clinical Development Specialist
Job typeMeditech
Salary GBP
Bonus Package
Job description

A market-leading developer of single use surgical instruments is currently looking for a Senior Post-Market Surveillance Specialist to join their team in Denmark and work on clinical post-market evaluation and development.

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.

As one of the largest providers of single use medical devices, they are supported by a strong research and development arm that is constantly innovating and collaborating with healthcare professionals on new products. Healthcare providers and patients around the world are positively impacted by their products!

The role

As Senior Post-Market Surveillance Specialist you will play an important role in post-market and clinical development activities for a range of products. You’ll be focused on clinical development of these products and will handle both vigilance reporting and clinical documentation associated with them. Working closely with these products, you will be able to share your clinical knowledge on how these can be developed post-market entry.

In this role you’ll join a team of likeminded individuals who are highly skilled in a growing department. You’ll work closely with this team and will work collaboratively to find success in projects, but you’ll also have to be confident in making decisions autonomously. If you’re looking for a professional challenge, this could be the perfect next step in your career.


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
  • Helping the team to understand levels of scientific and clinical documentation for new products
  • Planning and executing clinical evaluation of products
  • Support and guide other clinical staff in writing and documentation
  • Reviewing clinical documents
  • Enabling the demonstration of the value of clinical products in the market
  • Helping to bring new products to market quickly and effectively, in line with clinical and quality regulations



The requirements

You will live in the Greater Copenhagen area or within a commutable distance to it. You’ll be experienced in the clinical medical devices space, as well as…

  • A clinical background (ideally relating to anaesthesia, ICU or the OR)
  • Degree educated in a relevant clinical discipline
  • Knowledgeable in EU and FDA regulations and guidelines
  • A developmental mindset
  • Fast-paced and dynamic, able to zone in on what is important
  • Good commercial awareness
  • Experience working in clinical competence for medical device development projects
  • Able to take ownership of projects and work autonomously
  • Experience working collaboratively on projects
  • Strong written and verbal communication skills
  • Excellent English language skills (written and verbal)
  • A strategic thinker
  • Experience in clinical research



Important information

FMC contact for the role: Charlotte Ashton (

Reference number: 8923

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