Field Intervention Specialist, 70% Travel

Job not on LinkedIn

🔥 5 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $120k - $125.6k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 1%

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Teleflex

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🏭 Manufacturing

⚕️ Healthcare Insurance

💰 $275k Venture Round on 2010-01

Healthcare • Manufacturing • Healthcare Insurance

Teleflex is a global provider of innovative medical devices and solutions, dedicated to supporting healthcare professionals and enhancing patient care. With a diverse portfolio that includes products for anesthesia, emergency medicine, interventional cardiology, and more, Teleflex aims to improve the health and quality of lives. The company emphasizes its commitment to education and customer support in the healthcare sector.

📋 Description

• 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

• 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

• 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