Clinical Research Associate

5 days ago


Carlsbad, United States Meet Full time
Medical Device Clinical Trials Specialist

We are seeking a highly skilled Clinical Trials Specialist to join our team in the Medical Device industry. The ideal candidate will have a strong background in clinical research, regulatory affairs, and data management.

Key Responsibilities:

  • Conduct clinical evaluations and work directly with medical professionals to assess device performance and patient outcomes.
  • Ensure compliance with FDA regulations and ISO standards for clinical studies.
  • Collect, analyze, and report data to drive decision-making processes.
  • Collaborate with cross-functional teams to facilitate communication between clinical, engineering, and regulatory departments.
  • Experience in electrophysiology (EP) settings is a significant advantage.

Requirements:

  • At least 2 years of proven experience as a clinical CRA in the Medical Device industry.
  • Hands-on involvement in clinical evaluations and data management.
  • Strong knowledge of FDA regulations and ISO standards.
  • Effective communication and collaboration skills.

What We Offer:

A dynamic and challenging role in a growing industry, with opportunities for professional growth and development.



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