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Clinical Research Monitor

2 months ago

Columbus, Ohio, United States Edwards Lifesciences Full time

Join Edwards Lifesciences in a Rewarding Role

We are on a mission to enhance patient outcomes through groundbreaking medical technologies. We are looking for a Clinical Research Associate to join our dedicated Tricuspid team in the Midwest. If you are committed to safeguarding patient welfare during clinical studies, we invite you to explore this opportunity.

Key Responsibilities:

  • Conduct field monitoring of clinical studies and gather data for trials
  • Ensure accuracy of trial data and maintain essential regulatory documentation
  • Oversee trial operations and communicate findings to relevant stakeholders
  • Provide training on Good Clinical Practices (GCP), study protocols, and compliance with databases
  • Revise and update informed consent forms
  • Perform other related tasks as needed

Qualifications:

  • Bachelor's Degree in a relevant discipline
  • Minimum of 1 year experience in field monitoring or direct clinical research
  • Willingness to travel up to 75% for site visits
  • Covid Vaccination required

Preferred Skills:

  • Proficiency in Microsoft Office Suite
  • Knowledge of cardiovascular anatomy and physiology
  • Familiarity with medical device regulatory standards
  • Strong technical writing abilities
  • Experience with electronic data capture systems

At Edwards, we are committed to equal opportunity and affirmative action. Join us in our efforts to make a positive impact on patients' lives.