Edwards Lifesciences

Edwards Lifesciences

Senior Specialist, Clinical Education Imaging, Clinical Development

USA - California – Irvine · Senior · Full-time

Sponsorship not specified$134k-$190kDetected 67 days ago
ExcelClinical TrialsClinical ResearchMedical DevicesResearchCommunicationCollaborationProblem SolvingCritical ThinkingMicrosoft Office

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odds of building a lasting career here

61Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role90
Entry-level history0
PERM / green-card track0
Lottery odds (Level IV)94
Fits your clock70

Sponsors, but it's cap-subject — you still face the weighted lottery (~61% per draw at Level IV). Good if you win; have a cap-exempt backup on your list.

Lottery odds assume a STEM candidate.

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Employer immigration record

from this employer's Department of Labor filings

Green-card filing pattern in this occupation

Context, not a finding about this posting: of this employer's 14 green-card filings in this occupation, 100% were for a worker who already held the job.

Green-card follow-through: 50%

Of 10 labor certifications old enough to have been used, 5 expired without the employer filing the next step. Median time from filing to decision: 493 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.

Reported a layoff in this occupation

In a green-card filing decided 2026-06-04, this employer stated it had laid off workers in Quality Control Systems Managers (CA) during the preceding six months. 2 such filings on record.Describes the period before that filing, not necessarily today. Unlike WARN notices this is occupation-specific and federal.

Files H-1B transfers

3 transfer filings in the last year, covering 3 workers. Median labor-condition decision: 8 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

Community outcomes

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About the role

  • 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.

Responsibilities

  • Document procedural case observations for insights in investigating post procedural events. Support enrollment discussions and assistance with issue escalation with Principal Investigator and research team.
  • Develop, analyze, and optimize the design of more complex procedures, testing, and therapies leveraging substantial understanding of clinical imaging.
  • Create more complex design control and trial-related documentation and support all complaint and investigational analyses supporting the therapy.
  • Ability to manage competing priorities in a fast-paced environment
  • Work is performed independently on mid-to-large scale projects and will participate in determining objectives of assignment; plans schedules and arranges own activities in accomplishing objectives

Requirements

  • Provide expertise and clinical insights on the device, procedure, and protocol throughout the product life cycle from early studies through commercialization.
  • Must be willing to travel up to 50% nationwide
  • What you'll need (Required):
  • Must be able to work in a team environment, fostering collaboration between inter-departmental teams, HCPs and KOLs
  • Must be able to work in a team environment, including inter-departmental teams and key contact representing the organization on contracts or projects

Nice to have

  • What else we look for (Preferred):

Compensation

  • For California, the base pay range for this position is $134,000 - $190,000 (highly experienced).

Benefits

  • Substantial understanding of medical device regulatory requirements and documents, adverse events reporting

Company info

  • Join us and be part of our inspiring journey.
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This listing is sourced directly from Edwards Lifesciences's careers page and normalized into a canonical job model.