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 you'll 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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