Clinical Quality Expert
This position is responsible for ensuring the quality and integrity of our clinical research data.
Key responsibilities include:
* Maintaining our quality management system, including the development and updating of standard operating procedures (SOPs) and relevant documentation.
* Organizing training sessions for internal and external partners on regulatory requirements and best practices.
* Coordinating the submission and maintenance of clinical study information in international databases and registries.
* SUPPORTING THE TEAM IN QUALITY EVENT DOCUMENTATION AND AUDIT PREPARATION
To be successful in this role, you will need to have a strong understanding of regulatory requirements in the medical device industry. Experience with Microsoft Office and document management tools is an asset. Excellent communication skills, both written and verbal, are essential for effective collaboration with internal stakeholders and external partners.
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
BENEFITS OF WORKING WITH US:
* Flexible work arrangements
* A collaborative and dynamic work environment
* Opportunities for professional growth and development