Would you like to explore interesting clinical indications, work with exciting healthcare technology and help new medical devices go to market to benefit patients and health care professionals all over the world?
Are you having a passion for working with clinical documentation and clinical investigations? If you have a few years’ experience from the medical device industry and are eager to take responsibility and drive the necessary activities to document our medical devices, then we have an exciting job opportunity that may be your next career move…
Our customer develops, produces and sells medical devices, which enable doctors and nurses to save lives and improve patient care. They currently experience massive success and are looking for an additional Clinical Research Specialist to join their high-performing team.
We offer a challenging position where you will be an important player in the Clinical Research & Biosafety team placed under Global Innovation. You will participate in securing our ongoing dedication to quality products. You will be part of an effective innovation culture with a tradition for fast completion of projects, which means that there is a visible link between your results and the company growth.
You will join the Clinical Research & Biosafety team consisting of 15 colleagues. 11 based at the headquarters in Denmark, and four affiliated colleagues in Penang, Malaysia. This position can be based in either near Augsburg, Germany or Ballerup, Denmark. You will report to the Director of Corporate Clinical Research and Biosafety placed in Ballerup.
Setting the bar for clinical documentation and clinical investigations:
As Clinical Research Specialist, you will join a highly skilled and professional team. You will learn to set the right scientific level when implementing international clinical medical device legislation and regulation. This means that you, eventually, will be able to take responsibility to set the right documentation level and at the same time act as sparring partner in product development projects and improvement projects. You will, together with your mentor, plan how to balance your clinical scientific interest with a hands-on approach in the projects as you execute continuous clinical evaluation and post market clinical follow-up activities. As clinical specialists, one of your focus areas is to write and review clinical medical device documentation but also to execute accordingly. In due time, you will act as an expert in regulations and guidelines related to the clinical area. Together with the rest of the team, you will end up as a “go-to" person for the project members when setting the bar for clinical documentation.
A wish to be the expert in the clinical medical device area:
To succeed in this position, you need to hold an academic degree, e.g. a MSc in Health or similar, combined with a few years of experience from the medical device industry. You also need to have a genuine interest in being well versed in EU and FDA regulations and guidelines related to the clinical area. It will be an advantage if you have specific experience in working as the clinical competence in medical device development projects.
Finally, you need to have excellent command of the English language, as this will be your main working language, - verbally and in writing. German skills will be a further plus.
As a person, you enjoy working in a changing and challenging environment and you like to take the ownership for following through on changes. You are an efficient communicator and you are a very good networker as this will help you to succeed in the job. Additionally, you make accurate judgements and decisions and you feel a natural desire to drive continuous improvement.
A visionary and international workplace where your efforts matter:
Our customer is a company that expands rapidly and has ambitious growth targets. They meet these targets through interdisciplinary teamwork between motivated and highly skilled employees. Your contributions and efforts are crucial to the success and by joining the team you will get the opportunity to work in an international head office with an informal working environment.
The company offers a wide range of professional, social and financial employee benefits in addition to exciting job challenges and continuous professional and personal development.
Please apply in English!