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Senior Clinical Research Monitor - Remote

Posted 4 days ago
All others
Full Time
CA, USA
$106,000 - $140,000/year

Overview

The Senior Clinical Research Monitor will ensure trial patients' safety by assuring trials are conducted ethically and within regulatory compliance, focusing on data accuracy and protocol adherence.

In Short

  • Field monitoring of studies and data collection for clinical trials
  • Assess data documentation for consistency with case report forms
  • Monitor clinical trial safety in compliance with protocols and GCP
  • Develop and deliver technical training on GCPs and protocols
  • Act as a mentor to new or junior employees
  • Provide oversight of trial activities to principal investigators
  • Contribute to the development of clinical protocols and consent forms
  • Validate investigational device accountability
  • Verify trial/study data and maintain regulatory documents
  • Edit/amend informed consent documents

Requirements

  • Bachelor's Degree in related field or equivalent experience
  • 5 years of work experience in clinical research monitoring
  • Experience in a regulated industry
  • Experience with electronic data capture
  • Ability to travel up to 75% for clinical site visits
  • Covid Vaccination required

Benefits

  • Competitive salaries
  • Performance-based incentives
  • Variety of benefits programs

E.L

Edwards Lifesciences

Edwards Lifesciences is a global leader in patient-focused medical innovations, specializing in structural heart disease, critical care, and surgical monitoring. Headquartered in Irvine, California, the company is dedicated to addressing unmet healthcare needs through collaboration with leading clinicians and researchers. With over 15,000 employees worldwide, Edwards Lifesciences is committed to improving patient outcomes and enhancing lives by developing advanced medical devices and technologies. The company's mission is to help patients live longer and healthier lives, making a meaningful difference in healthcare.

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