
Job Overview
Location
USA-Massachusetts-Remote
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 7, 2026
Full Job Description
đź“‹ Description
- • As a Clinical Research Monitoring Specialist at Edwards Lifesciences, you will play a critical role in ensuring the integrity, safety, and compliance of clinical trials for transcatheter heart valve therapies, directly contributing to life-changing innovations that improve patient outcomes for those suffering from aortic stenosis.
- • Your day-to-day responsibilities include field monitoring of clinical studies, verifying data consistency with source documents, assessing protocol compliance, maintaining regulatory documentation, validating investigational device accountability, and providing training on GCPs, adverse event reporting, and study procedures to site staff and new employees.
- • You will work within the Clinical Affairs team, collaborating closely with principal investigators, medical professionals, patient advocacy groups, regulatory authorities, and internal stakeholders such as Clinical Operations and Contracts to drive evidence generation and recommend process improvements that enhance trial quality and efficiency.
- • In this role, you will deepen your expertise in clinical research monitoring, regulatory compliance (GCP, FDA, IEC), medical device accountability, and cardiovascular therapeutics, while developing leadership and training skills that support career advancement in clinical research or regulatory affairs within the medical device industry.
🎯 Requirements
- • Bachelor’s Degree or equivalent in a related field with 3 years of field monitoring, quality assurance/control, and regulatory compliance experience or equivalent work experience based on Edwards criteria.
- • Ability to travel up to 75% domestically.
- • Clinical research certification (ACRP or SoCRA clinical coordinator / CRA certification) – preferred.
- • Strong written and verbal communication, presentation, interpersonal, and analytical skills – preferred.
- • Proven expertise in MS Office Suite (Word, Excel, Adobe) and general computer software – preferred.
- • Demonstrated problem-solving and critical thinking skills – preferred.
🏖️ Benefits
- • Competitive salaries with a base pay range of $87,000 to $123,000 for Massachusetts-based candidates, depending on qualifications and experience.
- • Performance-based incentives tied to individual and company performance.
- • Wide variety of benefits programs addressing diverse individual and family needs, including health, wellness, and financial protections.
- • Equal Opportunity/Affirmative Action employer commitment, including support for protected veterans and individuals with disabilities.
- • Commitment to employee safety through COVID-19 vaccination requirements for patient-facing roles, with medical and religious accommodation options where permitted by law.
Skills & Technologies
About Edwards Lifesciences Corporation
Edwards Lifesciences Corporation, headquartered in Irvine, California, designs, manufactures, and markets medical devices for structural heart disease and critical care monitoring. Founded in 1958 and publicly traded on NYSE:EW, the company pioneered transcatheter aortic valve replacement and offers surgical heart valves, hemodynamic monitoring systems, and advanced catheter-based technologies. Its products serve hospitals and clinicians in more than 100 countries, focusing on improving patient outcomes in cardiovascular care.
Subscribe to the weekly newsletter for similar remote roles and curated hiring updates.
Newsletter
Weekly remote jobs and featured talent.
No spam. Only curated remote roles and product updates. You can unsubscribe anytime.
Similar Opportunities

Onelineage Inc.
23 days ago
28 days ago



