Clinical Study Manager

Do you see yourself as a project manager with a passion for conducting, planning and running clinical studies, improving lives through better biomarker data and building the next generation of diagnostics tools? Then this is the opportunity for you, join us as our new Clinical study manager.

About QLIFE

Qlife is a med-tech company that strives to revolutionize the market for clinical biomarker and virus tests. By enabling tests at home as a complement to tests in healthcare, access to important health information is facilitated, which can contribute to better treatment and potentially prevent diseases.

Our product The Egoo is a small, fist sized, portable device that analyzes tests. The tests can be made from either blood, plasma or mouth/nose swab depending on the specific test and takes 5-30 minutes for most tests. Results are qualitative or quantitative on par with existing laboratory tests. The tests are run from either smartphone or laptop and the results shown instantaneously. It is optional to share data with a GP, hospital or other caregiver – in accordance with GDPR regulation.

About The Team

The position of Clinical Study Manager resides in the R&D unit of our company, where you will be a part of a team of 17 colleagues as of date. We expect the team to grow substantially over the coming years and hope you will find great opportunities in supporting this journey. 

 

Our team is focused on innovation and creativity and for the most part is about finding new and better ways to improve our products. We solve problems together and even if we are working individually we help each other on a daily basis towards our common goals. 

The Process

Does this job offer interest you then apply with the form on this site as soon as possible with a resume and a cover letter. We are conducting interviews on an ongoing basis and we will not hesitate to hire the right candidate on the spot.

 

Should you have any questions regarding the position, the company or anything in between, please do not hesitate to contact Maiken W. Rosenstierne - MWR@egoo.health.

THE JOB

You will be responsible for the entire clinical project from initiation to completion of the clinical study. You will be responsible for the project management and deliverables of 1-3 studies/projects at a time. You will be responsible for protocol outline to the initiation of patient recruitment and you will oversee the studies. You will be accountable for the end-to-end planning, execution, and completion of the clinical studies. 

 

Your main responsibilities will be to:

  • Writing clinical study protocols in collaboration with our external clinical study sites

  • End-to-end planning and overseeing the clinical study

YOUR COMPETENCES

To succeed in the job, you need to have experience in writing clinical study protocols. Preferably from the medical device or other regulated industries.


We imagine that you: 

  • see yourself as a Project manager.

  • have excellent communications and presentation skills.

  • are structured.

  • have the ability to organize and motivate others.

  • and have excellent English skills (written and spoken).

YOUR PROFILE

We imagine that your professional background is within Natural Science and that you have four years of relevant experience. Relevant experience could be within: 

  • CRA

  • LTM

  • RTM

  • Study nurse

  • or CTA
     

It is important that you have a structured approach to your work, but at the same time, that you are open-minded and see possibilities. We imagine that you have a clear ability to maintain overview in a busy environment and you are a team player with the ability to also work independently.

 

It is natural for you to take charge and you are proactive, good at prioritizing, planning, and finalizing your tasks.

What we offer the right candidate

If you are our next Clinical study manager, working with clinical study management in Qlife, you are directly helping to pave the way for the Egoo Health System. 

The job is located at our facility in Ballerup, it is a full time position.


You will be working in an innovative and creative environment where we together want to make an impact towards our long term goal of giving people access to safe and validated biomarker data at home. You will become a part of a workplace where your work can help make a difference for the people who use our product.

 

As a colleague you will experience that we have a focus on creating a motivating environment within and across projects and teams - and last but not least having fun along the way. 

Let's Work Together

Apply here!