Edwards Lifesciences
Manager, Clinical Research Monitoring
Edwards Lifesciences, Saint Paul, Minnesota, United States
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 the organization
Competitive performance-based incentives and a wide variety of benefits programs
Chance to lead and mentor a team while working on groundbreaking innovations in structural heart technology
Ability to travel domestically and internationally, enhancing professional exposure and experience
Supportive and dynamic work environment that encourages innovation and personal development
What to Expect (Job Responsibilities)
Manage and lead a small team, including budget responsibilities and oversight of outside contractors/vendors
Provide strategic input on field monitoring of studies and data collection for clinical trials
Develop and deliver technical training on GCPs, protocols, and regulatory documentation requirements
Oversee clinical trial conduct, ensuring compliance and data entry accuracy
Participate in the development and validation of clinical protocols, informed consent forms, and case report forms
What is Required (Qualifications)
Bachelor's Degree in a related field with field monitoring experience, quality assurance/control, and regulatory compliance
Ability to travel up to 75% domestically and internationally
Proven experience in managing clinical trials and understanding of regulatory requirements
Strong problem-solving, organizational, analytical, and critical thinking skills
Excellent written and verbal communication skills
How to Stand Out (Preferred Qualifications)
8+ years of related experience in cardiology trials
Master’s Degree in a related field
Clinical research certification (ACRP or SoCRA clinical coordinator/CRA certification)
Proficiency in trial management systems (e.g., RAVE, CTMS, Veeva)
Strong understanding of ISO 14155, FDA, and international regulatory requirements
#MedicalDevices #ClinicalResearch #HealthcareInnovation #CareerGrowth #LeadershipOpportunity
We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.
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Why consider this job opportunity
Salary up to $174,000 for highly experienced candidates
Opportunity for career advancement and growth within the organization
Competitive performance-based incentives and a wide variety of benefits programs
Chance to lead and mentor a team while working on groundbreaking innovations in structural heart technology
Ability to travel domestically and internationally, enhancing professional exposure and experience
Supportive and dynamic work environment that encourages innovation and personal development
What to Expect (Job Responsibilities)
Manage and lead a small team, including budget responsibilities and oversight of outside contractors/vendors
Provide strategic input on field monitoring of studies and data collection for clinical trials
Develop and deliver technical training on GCPs, protocols, and regulatory documentation requirements
Oversee clinical trial conduct, ensuring compliance and data entry accuracy
Participate in the development and validation of clinical protocols, informed consent forms, and case report forms
What is Required (Qualifications)
Bachelor's Degree in a related field with field monitoring experience, quality assurance/control, and regulatory compliance
Ability to travel up to 75% domestically and internationally
Proven experience in managing clinical trials and understanding of regulatory requirements
Strong problem-solving, organizational, analytical, and critical thinking skills
Excellent written and verbal communication skills
How to Stand Out (Preferred Qualifications)
8+ years of related experience in cardiology trials
Master’s Degree in a related field
Clinical research certification (ACRP or SoCRA clinical coordinator/CRA certification)
Proficiency in trial management systems (e.g., RAVE, CTMS, Veeva)
Strong understanding of ISO 14155, FDA, and international regulatory requirements
#MedicalDevices #ClinicalResearch #HealthcareInnovation #CareerGrowth #LeadershipOpportunity
We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.
#J-18808-Ljbffr