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!
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