Clinical Trial Coordinator

Are you passionate about advancing clinical studies for cutting-edge medical devices? Do you thrive in dynamic, fast-paced environments?

We are seeking a Clinical Research Associate to join an innovative, world-class medical technology company. In this role, you will design, plan, and execute both pre-market and post-market clinical studies, ensuring compliance with protocols and regulations.

What will you do?

• Develop and manage clinical study documents and processes.
• Oversee ethics submissions and trial master files.
• Perform site visits and monitoring, ensuring data accuracy and compliance.
• Collaborate with cross-functional teams and external stakeholders

What we’re looking for:

• Bachelor’s degree in Science or related field with 4+ years in the medical device industry.
• Proven experience in pre-market and post-market clinical studies.
• Expertise in ISO 13485, ISO 14155, ICH GCP, EU MDR, and US 21 CFR 820.
• Exceptional organisational and communication skills.

This is your chance to join a team dedicated to making a meaningful impact in healthcare. If you are detail-oriented, self-motivated, and thrive in entrepreneurial settings, we want to hear from you!