[Hiring] Field Intervention Specialist @Teleflex

Role Description

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.

Qualifications

• 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.

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.

Benefits

• Medical, prescription drug, dental and vision insurance.
• Flexible spending accounts.
• Participation in 401(k) savings plan.
• Various paid time off benefits, such as PTO, short- and long-term disability, and parental leave.