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Manager, Clinical Research Monitoring

Job in Murfreesboro, Rutherford County, Tennessee, 37132, USA
Listing for: Edwards Lifesciences
Full Time position
Listed on 2026-02-28
Job specializations:
  • Healthcare
    Medical Science, Clinical Research
Salary/Wage Range or Industry Benchmark: 174000 USD Yearly USD 174000.00 YEAR
Job Description & How to Apply Below

Employer Industry: Medical Device and Healthcare Innovation

Why consider this job opportunity:
  • Salary up to $174,000 for highly experienced candidates
  • Opportunity for career advancement and growth within a leading medical technology company
  • Comprehensive benefits programs tailored to meet diverse employee needs
  • Supportive and collaborative work environment focused on innovation
  • Chance to make a significant impact on patient outcomes through groundbreaking clinical trials
  • Ability to travel domestically and internationally, enhancing professional experience
What to Expect (Job Responsibilities):
  • Manage and lead a small team, including budget responsibilities and oversight of contractors/vendors
  • Provide strategic input on field monitoring of clinical trials and data collection, ensuring compliance with protocols and regulatory requirements
  • Develop and deliver technical training on Good Clinical Practices (GCPs) and study-related activities
  • Oversee clinical trial conduct, including management of metrics, compliance, and protocol deviations
  • Identify and evaluate opportunities for clinical process improvement
What is Required (Qualifications):
  • Bachelor's Degree in a related field with experience in field monitoring, quality assurance/control, and regulatory compliance
  • Ability to travel up to 75% domestically and internationally
  • Proven expertise in managing clinical trials and ensuring compliance with regulatory standards
  • Strong written and verbal communication skills, including negotiation and relationship management
  • Excellent problem-solving and analytical skills
How to Stand Out (Preferred Qualifications):
  • 8+ years of experience in cardiology trials
  • Master’s Degree in a related field or clinical research certification (ACRP or SoCRA)
  • Strong understanding of ISO 14155, FDA, and international regulatory requirements
  • Proficiency in trial management systems (e.g., RAVE, CTMS, Veeva)
  • Demonstrated leadership skills in project management and team development

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