Clinical Project Manager
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 www.qmed-consulting.com. 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 project manager with experience. This position can be based in a European country. The candidate must be proficient in both written and spoken English.
Your main responsibilities will include but are not limited to:
As a Clinical Project Manager you are responsible for the successful execution of clinical trials from the protocol concept through to the clinical study report. The CPM manages all aspects of the study ensuring completion of study deliverables, and typically works on studies with moderate to high complexity. You should be able to proactively identify and resolve clinical project issues. You will ensure that project deliverables and milestones are met in time, at a high quality and within budget. You will be responsible for a multicultural, remote team as well as other stakeholders globally (eg data management, statistics). You may be expected to help with monitoring 1-2 sites if assistance is required on site.
What we look for in a candidate:
You hold a university degree in life-science or equivalent, or have a medical background and have substantial knowledge and a proven track record of at least 2-3 years of excellent performance in project management, covering all aspects of clinical trial methodology and trial management.
You are a dedicated team player who motivates your team to deliver their best in an ever-changing environment. You know how to prioritise between different tasks in a dynamic environment which requires a high degree of flexibility. By use of clear communication and strong presentation skills you inspire trust among your colleagues as well as your Clients.
Sounds like you?
- You have excellent organisational and prioritisation skills and good attention to detail.
- You have excellent communication skills and you aim to reach deadlines, are proactive, flexible, and able to multi-task.
- You have solid IT skills 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.
- You understand clinical trial processes and needs, including knowledge of ICH GCP and/or ISO 14155.
If you have any questions regarding the position, you are welcome to contact us at +45 56 64 1010 or email@example.com.
Start date is as soon as possible, but we will wait for the right candidate.
We look forward to hearing from you.