
Senior Analyst, Clinical Patient Screening, TMTT
Multiple U.S. locations · FlexibleFull-time$92–130K/yrSeen todaySeen in employer's feed today
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At a glance
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Job overview
The Senior Analyst, Clinical Patient Screening coordinates and manages case-planning workflows for Edwards Lifesciences’ TMTT US commercial team. The role supports technical platforms, stakeholder communication, imaging submissions, project-management tasks, and process improvement to prepare the field team for procedural outcomes. Candidates may work onsite in Irvine, California, or remotely from the US, with occasional travel to Irvine for training and department meetings.
Skills & qualifications
Skills
Qualifications
Full job description
#LI-REMOTE
USA - California – Irvine
Full time
Req-51916
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient’s unmet clinical needs. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
The Senior Analyst, Clinical Patient Screening will coordinate and manage case planning workflows for the Transcatheter Mitral & Tricuspid Therapies (TMTT) US commercial team. This position will play a key role in launching and supporting the case planning needs to prepare the US field team for achievement of exceptional procedural outcomes.
Role is open to onsite (local to Irvine CA) or remote US based candidates. Occasional travel for training and department meetings at Irvine CA corporate headquarters required if employed remotely.
How you’ll make an impact:
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Oversee daily requests and support for the technical platforms used for case planning activity in partnership with the field team, case planning, sales operations, information technology and external stakeholders.
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Responsible for collaborating with the case planning team to plan, schedule, track, manage and achieve defined goals.
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Responsible for external stakeholder communication and support for the case planning workflow process.
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Coordinate project management platform tasks and process standardization.
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Drive timely and accurate imaging submissions from commercials sites to allow for internal review by the case planning team.
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Identify issues and provide recommendations for process improvement.
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Provide high quality, timely responses to the sales organization to meet information and reporting needs. Communicate complex logic and analysis in a manner that is easily understandable.
What you’ll need (required):
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Bachelor's Degree in related field (Biology, Lifesciences, etc) or equivalent work experience based on Edward’s criteria required
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Minimum 5 years’ experience in patient screening in clinical trial or clinical research environment
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Certified Clinical Research Professional (SOCRA) preferred
What else we look for (preferred):
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Proficient with Microsoft Office Suite (Word, Excel, PowerPoint, CoPilot etc)
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Exhibits professional communication and interpersonal relationship skills
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Demonstrates problem-solving, organizational, analytical, and critical thinking skills
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Moderate understanding of medical terminology as it relates to clinical studies
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Ability to manage confidential information with discretion
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Strict attention to detail
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Ability to interact professionally with all organizational levels
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Thrives in a cross functional, collaborative team environment, including inter-departmental teams and representing the organization on specific projects
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Ability to build productive internal/external working relationships
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Commitment to following all company policies and requirements, including Environmental Health & Safety guidelines
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California, the base pay range for this position is $92,000 - $130,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.
How this job compares
Set against the 1,405 open Clinical Research jobs on Olive Jobs, counted November 6, 2026.
- Pay
- This posting$92–130K/yr
- US median$118–190K/yr715 salary ranges
This range's midpoint, $111K, is 25% below the US median midpoint ($148K) — in the middle half of Clinical Research salary ranges across the US.
- Openings
- Olive Jobs lists 1,405 open Clinical Research jobs across the US. 15% of them nationwide are listed as remote or flexible.
- Hiring the most across the US
- IQVIA100 open
- Merck71 open
- Edwards Lifesciences (this employer)61 open
- Experience
- This posting asks for at least 5 years of experience; Clinical Research postings that state a minimum ask for 3 years at the median (1,029 postings).
- Education
- 563 of the 1,405 open Clinical Research jobs (40%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 6, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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