Position 3737
Responsible for planning and execution of the companys clinical targets.
Prepare and manage PMCF records, plans, and reports in alignment with regulatory requirements.
Conduct data collection and analysis to ensure the safety and efficacy of our products.
Generate comprehensive PMS reports.
Coordinate and oversee ongoing clinical studies, ensuring adherence to Good Clinical Practice (GCP) standards.
Work collaboratively with investigators and study sites to maintain
timelines and quality standards and more.
Requirements: Masters degree in life sciences, biomedical engineering
Previous experience in clinical research with medical devices
GCP certified
Proficient in Excel
High level English proficiency, speaking and writing
This position is open to all candidates.