Clinical Research Specialist
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Ballerup
Would you like to explore interesting clinical indications and work with exciting healthcare technology? Would you like to help new medical devices go to market to benefit patients and health care professionals? And, do you have a passion for working with clinical documentation and clinical investigations? Then we have an exciting job opportunity that may be your next career move…
At Ambu, we develop, produce and sell medical devices, which enable doctors and nurses to save lives and improve patient care. We currently experience massive success and are looking for an additional Clinical Research Specialist to join our high-performing team.
We are looking for new colleagues with a few years of experience from the medical device industry who is eager to take responsibility and drive the necessary activities to continuously document our medical devices. We offer a challenging position where you will be an important player in the brand-new function, Post Market Clinical Development in Clinical Research & Biosafety 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 Ambu’s growth.
You will join the Clinical Research & Biosafety team consisting of 18 colleagues. 14 colleagues are based at Ambu’s headquarters in Ballerup, Denmark, and four affiliated colleagues in Penang, Malaysia.
You will report to the Manager of Post Market Clinical Development 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 set the scientific level when implementing international clinical medical device legislation and regulation during the post market phases of our products. This means that you will take responsibility to set the right documentation level and at the same time act as sparring partner in incremental development projects and improvement projects.
You will have to 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. At the same time, you will support in strengthening the clinical commercial foundation for our marketed products.
As a clinical specialist, one of your focus areas is to write and review clinical medical device documentation but also to execute on post market clinical follow up plans. In due time, you will act as an expert in regulations and guidelines related to the post market clinical area. Together with the rest of the team, you will end up as a “go-to" person for our colleagues when it comes to 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, preferably 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 a medical device company.
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. You enjoy working with and follow-up on plans to ensure that projects are completed. Additionally, you make accurate judgements and decisions and you feel a natural desire to drive continuous improvement.
Finally, you need to have excellent command of the English language, as this will be your main working language, - verbally and in writing.
Ambu – a visionary and international workplace where your efforts matter
Ambu is a company that expands rapidly and has ambitious growth targets. We meet these targets through interdisciplinary teamwork between motivated and highly skilled employees. Your contributions and efforts are crucial to our success and by joining us you will get the opportunity to work in an international head office with an informal working environment.
We offer a wide range of professional, social and financial employee benefits in addition to exciting job challenges and continuous professional and personal development.
When to apply
If you are interested in the position, then please apply as soon as possible. This job ad might be online until 7 August 2019.
If you have any questions about the position, you can contact Helene Gustafsson, Director of Clinical Research and Biosafety, telephone +45 7225 2000.
Your application will be treated with confidentiality.
At Ambu, we develop, produce and sell medical devices, which enable doctors and nurses to save lives and improve patient care. We currently experience massive success and are looking for an additional Clinical Research Specialist to join our high-performing team.
We are looking for new colleagues with a few years of experience from the medical device industry who is eager to take responsibility and drive the necessary activities to continuously document our medical devices. We offer a challenging position where you will be an important player in the brand-new function, Post Market Clinical Development in Clinical Research & Biosafety 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 Ambu’s growth.
You will join the Clinical Research & Biosafety team consisting of 18 colleagues. 14 colleagues are based at Ambu’s headquarters in Ballerup, Denmark, and four affiliated colleagues in Penang, Malaysia.
You will report to the Manager of Post Market Clinical Development 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 set the scientific level when implementing international clinical medical device legislation and regulation during the post market phases of our products. This means that you will take responsibility to set the right documentation level and at the same time act as sparring partner in incremental development projects and improvement projects.
You will have to 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. At the same time, you will support in strengthening the clinical commercial foundation for our marketed products.
As a clinical specialist, one of your focus areas is to write and review clinical medical device documentation but also to execute on post market clinical follow up plans. In due time, you will act as an expert in regulations and guidelines related to the post market clinical area. Together with the rest of the team, you will end up as a “go-to" person for our colleagues when it comes to 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, preferably 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 a medical device company.
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. You enjoy working with and follow-up on plans to ensure that projects are completed. Additionally, you make accurate judgements and decisions and you feel a natural desire to drive continuous improvement.
Finally, you need to have excellent command of the English language, as this will be your main working language, - verbally and in writing.
Ambu – a visionary and international workplace where your efforts matter
Ambu is a company that expands rapidly and has ambitious growth targets. We meet these targets through interdisciplinary teamwork between motivated and highly skilled employees. Your contributions and efforts are crucial to our success and by joining us you will get the opportunity to work in an international head office with an informal working environment.
We offer a wide range of professional, social and financial employee benefits in addition to exciting job challenges and continuous professional and personal development.
When to apply
If you are interested in the position, then please apply as soon as possible. This job ad might be online until 7 August 2019.
If you have any questions about the position, you can contact Helene Gustafsson, Director of Clinical Research and Biosafety, telephone +45 7225 2000.
Your application will be treated with confidentiality.
Information og data
Denne ledige stilling har jobtypen "Kemiker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Ballerup.
Jobbet er oprettet på vores service den 30.7.2019, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Kemiker
- Ballerup
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