Field Intervention Specialist (REMOTE- 70% travel)

Position Summary

The Field Vascular Intervention Specialist is a position that provides field support for clinical studies involving both peripheral vascular and coronary products, including product-specific and clinical protocol training, data collection, and study device implant participation. The incumbent will support efforts to promote medical acceptance of vascular intervention products and serve as a field technical expert on the study device.

Principal Responsibilities

• 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.

Education / Experience 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 the field of vascular intervention, preferably peripheral or cardiac stents.
• Minimum of three years’ clinical experience in the Cardiac Catheterization Lab is required.

Specialized Skills / Other Requirements

• Experience with one or more phases of clinical studies (start-up, management, closure), either with Teleflex or another company.
• Ability to manage multiple projects concurrently.
• Strong working knowledge and understanding of FDA, ICH, and GCP regulations governing clinical trials, 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.
• Demonstrate aptitude in and knowledge of relevant therapeutic areas and ability to learn and integrate new/different therapeutic areas.

• Ability to work independently and as a part of a team.
• Excellent communication, presentation, interpersonal, and computer skills.
• Excellent organizational skills and attention to detail.

CULTURE:
• Customer Experience – Representing Teleflex in a customer-facing position is a tremendous responsibility and opportunity. All CMA colleagues are expected to perform with the highest levels of professionalism, service, and ethics in order to strengthen the Teleflex brand and relationship with our customers.
• Continuous Improvement - Demonstrates initiative and critical thinking to identify and prioritize process and performance gaps. Develops solutions to deliver improved results. Exemplifies continuous improvement of thought processes and focus.
• Culture and Values – Exemplifies Teleflex values and ensures a fair, open, and productive climate that is engaging, ethical, and legally compliant. Strives to work effectively across boundaries in a complex matrix environment. Leads and participates in the process of promotional and other materials, working
internally and cross-functionally to ensure materials are processed completely, based on accurate interpretation of clinical practice and data.

TRAVEL REQUIRED: 70%

The pay range for this position at commencement of employment is expected to be between $120,000- $125,600 however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position will also include benefits such as medical, prescription drug, dental and vision insurance, flexible spending accounts, participation in 401(k) savings plan, and various paid time off benefits, such as PTO, short- and long-term disability and parental leave, dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.

If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.