Clinical Team Manager

Copenhagen, Hovedstaden

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 allow them entry to the market. Find out more on We value an open, trust-based and creative working environment, great team spirit and a high quality mind-set. Our working environment is characterised by 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 team manager with experience. This position is based in the Copenhagen office. The candidate must be proficient in both written and spoken English.

Your main responsibilities will include but are not limited to:

Oversight and point of contact for the clinical team in the office/in Denmark
Participate and present at bid-defence meetings and customer meetings
Communicate actively with project team and stakeholders
Contribute to the development and review of clinical procedures
Act as back up for project managers and monitors on projects when needed
Responsible for the production in the team

Personal competences:

Able to show initiative
Able to work independently
Plans ahead and is organised and systematic
Very good collaboration skills
Ability to create good relations with customers
A natural role model for the team members

Desired qualifications:

Relevant Academic qualification or medical background
Minimum of two years of experience preferable in medical device CRO
Minimum of two years’ experience managing a team
Experience from the CRO industry is a plus
Experience from the clinical field
Broad knowledge of therapeutic areas
Broad and in-depth knowledge of clinical trials including corresponding legislation and best practice
Awareness of QMS practices
Excellent communication skills
Excellent MS skills and basic knowledge of statistics
High English skills (oral and writing)

Sounds like you?

If you have any questions regarding the position, you are welcome to contact us at +45 56 64 1010 or
Start date is as soon as possible, but we will wait for the right candidate.

We look forward to hearing from you.

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