Field Intervention Specialist, 70% Travel

Teleflex

. Establish and maintain clinical trial sites for interventional cardiology studies (coronary and peripheral) .

Posted 10/23/2026full-timeRemote • North Carolina • United StatesMid-LevelSenior💰 $120,000 - $125,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials for interventional cardiology, ensuring compliance with FDA, ICH, and GCP regulations. Proven ability to train personnel, support device implants, and enhance clinical processes while maintaining strong professional relationships with investigators and sites.

Highest-signal resume keywords

Clinical Trial ManagementCardiac Catheterization Lab ExperienceFDA, ICH, and GCP Regulations KnowledgeData Collection and ComplianceProject Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study SupportData CollectionRegulatory ComplianceBiostatisticsMedical Device SupportClinical Protocol TrainingProcess ImprovementLogistical Issue ResolutionInterventional Cardiology KnowledgeTherapeutic Area Integration

Soft Skills

Excellent CommunicationInterpersonal SkillsOrganizational SkillsAttention to DetailTeam Collaboration

Industry Keywords

Clinical TrialsVascular InterventionPeripheral StentsCardiac StentsClinical ResearchIDE Clinical StudiesStudy ProtocolsSite CoordinationInvestigational DevicesQuality Improvement Initiatives

About the role

Key responsibilities & impact

Establish and maintain clinical trial sites for interventional cardiology studies (coronary and peripheral)
Train site personnel and investigators on study devices and clinical protocols
Provide technical and clinical support during device implants and follow-ups
Serve as a resource for site coordinators, investigators, and field personnel
Ensure accurate and complete data collection in compliance with study protocols
Assist in timely data collection and submission to meet protocol requirements
Develop and maintain professional relationships with investigators and sites
Identify, escalate, and resolve logistical and operational issues during study execution
Report and address serious protocol compliance issues
Support onboarding and training of newly hired specialists as needed
Support quality improvement initiatives
Contribute to process and procedure enhancements under the direction of clinical management
Represent Teleflex professionally in customer-facing interactions
Work internally and cross-functionally on promotional and other materials

Requirements

What you’ll need

Bachelor’s degree in a health, science, or engineering field preferred; candidates with an Associate degree may be considered with 3+ years of directly relevant experience
Minimum of three years’ experience supporting clinical studies on behalf of industry in vascular intervention, preferably peripheral or cardiac stents
Minimum of three years’ clinical experience in the Cardiac Catheterization Lab required
Experience with one or more phases of clinical studies (start-up, management, closure)
Ability to manage multiple projects concurrently
Strong working knowledge of FDA, ICH, and GCP regulations governing clinical trials
Knowledge of standard regulatory and clinical practices and current regulatory issues related to clinical research
Additional experience in clinical settings, biostatistics, IDE clinical studies, or medical device product support
Knowledge of relevant therapeutic areas and ability to learn and integrate new/different therapeutic areas
Ability to work independently and as part of a team
Excellent communication, presentation, interpersonal, and computer skills
Excellent organizational skills and attention to detail
Willingness and ability to travel 70%

Benefits

Comp & perks

Medical insurance
Prescription drug insurance
Dental insurance
Vision insurance
Flexible spending accounts
401(k) savings plan
Paid time off (PTO)
Short-term disability
Long-term disability
Parental leave