Field Intervention Specialist, 70% Travel

This is a fully remote position, open to applicants in North Carolina.

📋 Description

• Set up and oversee clinical trial sites for interventional cardiology studies, including coronary and peripheral procedures.

• Educate site personnel and investigators on study devices and clinical protocols.

• Offer technical and clinical assistance during device implantations and follow-up visits.

• Act as a resource for site coordinators, investigators, and field staff.

• Ensure precise and comprehensive data collection in accordance with study protocols.

• Aid in the prompt collection and submission of data to fulfill protocol requirements.

• Build and sustain professional relationships with investigators and study sites.

• Identify, escalate, and resolve logistical and operational challenges throughout the study execution.

• Report and address any serious protocol compliance concerns.

• Assist with the onboarding and training of newly hired specialists as necessary.

• Support initiatives aimed at quality improvement.

• Contribute to the enhancement of processes and procedures under the guidance of clinical management.

• Represent Teleflex in a professional manner during customer interactions.

• Collaborate internally and cross-functionally on promotional and other materials.

⛳️ Requirements

• A Bachelor’s degree in a health, science, or engineering discipline is preferred; candidates with an Associate degree may be considered if they have 3+ years of directly relevant experience.

• At least three years of experience supporting clinical studies in the vascular intervention field, ideally related to peripheral or cardiac stents.

• A minimum of three years of clinical experience in a Cardiac Catheterization Lab is required.

• Familiarity with one or more phases of clinical studies, including start-up, management, and closure.

• Capability to manage multiple projects simultaneously.

• Strong understanding of FDA, ICH, and GCP regulations governing clinical trials.

• Knowledge of standard regulatory and clinical practices, along with current regulatory issues relevant to clinical research.

• Additional experience in clinical environments, biostatistics, IDE clinical studies, or medical device product support is beneficial.

• Awareness of pertinent therapeutic areas and the ability to learn and integrate new or different therapeutic areas.

• Ability to work both independently and collaboratively within a team.

• Exceptional communication, presentation, interpersonal, and computer skills.

• Outstanding organizational skills and meticulous attention to detail.

• Willingness and ability to travel up to 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.