Qmed Consulting A/S is a full-service medical device Contract Research Organisation (CRO), also providing strategic consulting services. We specialise within medical devices, in the following departments:

•   Clinical Affairs
•   Regulatory Affairs
•   Quality Management
•   Commercial Healthcare

The driving force behind Qmed Consulting is our commitment to paving the way for new medical devices and new ideas to enable them access to the market. Find out more on www.qmed-consulting.com. We value an open, trust-based and creative working environment, great team spirit and a high quality mind-set. Our work day is made up of interesting and demanding assignments. We offer a career in clinical trials, where you will be challenged every day in a friendly and exciting work environment.
Qmed Consulting is looking for a clinical research associate to cover Germany. The applicant must be fluent in German with good written skills. They must also be proficient in both written and spoken English.

Your main responsibilities will include but are not limited to:
As a Clinical Research Associate you are responsible for the management and monitoring of the clinical study centres. You will be involved in the submission process to gain approval from the Ethics Committee and Competent Authority. You will need to work with different electronic data capture systems. You will work with the Project Manager to ensure that project deliverables and milestones are met in time, at a high quality and within budget. At Qmed we have a multicultural, remote and office based team as well as other global stakeholders (eg data management, statistics).

What we look for in a candidate:

You hold a university degree in life-science or equivalent, or have a medical background or a training in clinical trials. You are able to work in a quick changing environment and demonstrate flexibility to allow prioritisation of urgent tasks. You are a team player who can also work independently when required.

You have good organisational and prioritisation skills and good attention to detail.
You have good communication skills and you aim to reach deadlines, are proactive, flexible, and able to multi-task.
You are able to work with different IT systems and work in an organized manner with an attention to details.
It is essential that you can work independently, but also be an active contributor within a team.
You have the ability and willingness to adjust quickly to new situations in a continuously developing environment.

Sounds like you?
If you have any questions regarding the position, you are welcome to contact us at sjo@qmed-consulting.com.

Start date is as soon as possible, but we will wait for the right candidate.

We look forward to hearing from you.