Our partner is a pioneering medical device company focused on developing advanced imaging solutions with the potential to revolutionize cancer surgery and improve patient care.
Their technology enables real-time cancer tissue identification, supporting immediate surgical intervention and opening new possibilities for diagnostic and therapeutic applications.
To support their ongoing growth, we are currently seeking a Clinical Study Manager based at headquarters in Liège, Belgium.
Responsibilities
As Clinical Study Manager, you are responsible for the coordination of all clinical studies in Europe.
These are your responsibilities :
- You will manage clinical studies in Europe in collaboration with internal and external partners.
- Ensure that studies comply with GCP standards and regulatory requirements.
- Develop and maintain essential documents and structures for efficient study execution.
- Address site-specific requests and resolve any product-related issues.
- Secure all necessary regulatory and ethics approvals.
- Guide and train CRAs/CROs on study protocols and procedures.
- Oversee data collection and ensure timely entry according to study protocols.
- Report project progress and results regularly to your line manager.
Profile
- Hold a Bachelor’s degree in a health-related field, with 5-10 years of experience in clinical trial management, ideally in medical devices.
- Possess knowledge of clinical research regulations.
- Demonstrate strong communication, organizational, and problem-solving skills.
- Be able to work independently, with strong attention to detail.
- Have project management skills and a customer-oriented approach.
- Be fluent in English (written and oral); French is a plus.
- Be willing to travel up to 40%
Offer
- A stimulating and varied position within a fast-growing, innovative medtech company.
- Training in Switzerland to support your integration and development.
- An opportunity to contribute to the growth of a high-potential medtech company.
- A collaborative, dynamic, and professional work environment with international exposure and development opportunities.
- An attractive compensation package aligned with the role and your experience.
Your application and related information will remain strictly confidential.