Be a part of ouR team

Are you a medical device expert in search of a new challenge? If so, we would really like to meet you.

At Devicia, our focus is to deliver the best possible service and expertise for our clients. We are passionate about what we do and to always stay one step ahead. Together we enable safe medical devices for patients all over the world.

Feel free to send us a spontaneous job application.

VACANT POSITIONS

Clinical Research Manager - IVDs and Medical Devices

We are Devicia – a fast expanding global CRO solely focused on Medical Devices and In Vitro Diagnostics with offices in Lund, Gothenburg, Stockholm, Sweden and the U.S.

 We are a part of a strong group of five partner companies. Together we support our clients throughout the complete life cycle of their medical devices and in vitro diagnostics – from idea and market access to post-market surveillance and follow-up. The demand for our services is high and we are therefore seeking new team members to join our Clinical Affairs team.  

 You will work in a cross-functional group of highly skilled and experienced experts where you will help our clients navigate the regulatory landscape. Whether our clients need assistance with finding a suitable notified body, entering new markets, collecting clinical, or making the transition to the new Medical Devices Regulations, we are there to support. As part of our team, you will be given the freedom of running projects, defining, and developing your own role. 

We are looking for an individual with vast experience within clinical affairs and clinical research management. You have an advanced degree in a relevant scientific discipline. The most important ability is, however, that you want to be a part of our team with a will to grow and develop together with our companies.

 If you appreciate working in an agile and client-focused workplace with a lot of passion, you will enjoy working at Devicia. In this role you will be working from one of our offices (hybrid), preferably in Stockholm, Mölndal, or Lund – but the right candidate can be placed elsewhere.

Please send your CV and Cover Letter to recruitment@devicia.com and contact +46 72 555 68 91 if you have any questions. Applications will be reviewed on a rolling basis. 

IVD Expert

We are Devicia – a fast expanding global CRO solely focused on Medical Devices and In Vitro Diagnostics with offices in the US and Sweden.

 We are part of a strong group of five partner companies. Together we support our clients throughout the complete life cycle of their medical devices and in vitro diagnostics – from idea and market access to post-market surveillance and follow-up. The demand for our services is high and we are therefore seeking new team members to join our In Vitro Diagnostics team.  

You will work in a cross-functional group of highly skilled and experienced experts where you will help our clients navigate the regulatory landscape. Whether our clients need assistance with finding a suitable notified body, entering new markets, collecting clinical performance data, or making the transition to the new In Vitro Diagnostic Medical Devices Regulation, we are there to support. As part of our team, you will be given freedom of running projects, defining, and developing your own role.

We are looking for an individual with vast experience within In Vitro Diagnostics, clinical and/or regulatory affairs, medical writing, or clinical research management. You have an advanced degree in a relevant scientific discipline. The most important capacity is, however, that you want to be a part of our team with a will to grow and develop our companies.

If you appreciate working in an agile and client-focused workplace with a lot of passion, you will enjoy working at Devicia. In this role you will be working from one of our offices (hybrid), preferably in Stockholm, Mölndal, or Lund – but the right candidate can be placed elsewhere.

Please send your CV and Cover Letter to recruitment@devicia.com and contact +46 72 555 68 91 if you have any questions.

Clinical Research Manager

We are Devicia – a fast expanding global CRO solely focused on Medical Devices and In-Vitro Diagnostics with offices in the US and Sweden.

We are part of a strong group of six partner companies. Together we support our clients throughout the complete life cycle of their medical devices – from idea and market access to post-market surveillance and follow-up. The demand for our services is high and we are therefore seeking new team members to join our clinical and regulatory team.

As part of a cross-functional group of experts you will help our clients navigate the regulatory landscape. Whether our clients need assistance with finding a suitable notified body, entering new markets, collecting clinical data, or making the transition from the medical device directive to the new medical device regulation, we are there to support. Being part of our team you will be given freedom of running projects, defining, and developing your own role.

We are looking for an individual with vast experience within clinical and/or regulatory affairs, medical writing, or clinical research management. You have an advanced degree in a relevant scientific discipline. The most important capacity is, however, that you want to be a part of our team with a will to grow and develop our companies.

If you appreciate working in an agile, and client-focused workplace with a lot of passion you will enjoy working at Devicia. In this role you will be working from one of our offices, preferably in Stockholm or Mölndal – but the right candidate can be placed elsewhere.

Please send your CV and Cover Letter to recruitment@devicia.com or contact +46 72 555 68 91 if you have any questions.

Join our team!

We are Devicia – a fast expanding global CRO solely focused on Medical Devices and In-Vitro Diagnostics with offices in the US and Sweden. We are part of a strong group of six partner companies. Together we support our clients throughout the complete life cycle of their medical devices – from idea and market access to post-market surveillance and follow-up. The demand for our services is high and we are therefore seeking new team members to join our clinical and regulatory team.  

As part of a cross-functional group of experts you will help our clients navigate the regulatory landscape. Whether our clients need assistance with finding a suitable notified body, entering new markets, collecting clinical data, or making the transition from the medical device directive to the new medical device regulation, we are there to support. Being part of our team you will be given freedom of running projects, defining, and developing your own role.

We are looking for an individual with vast experience within clinical and/or regulatory affairs, medical writing, or clinical research management. You have an advanced degree in a relevant scientific discipline. The most important capacity is, however, that you want to be a part of our team with a will to grow and develop our companies.  

If you appreciate working in an agile, and client-focused workplace with a lot of passion you will enjoy working at Devicia. In this role you will be working from one of our offices, preferably in Stockholm or Mölndal – but the right candidate can be placed elsewhere. 

Please send your CV and Cover Letter to recruitment@devicia.com