Remote Field Clinical Specialist, Vascular Trials

Abbott; Springfield (IL); Remote; USD 61,000 - 123,000; Full time

Benefits offered by this job

Career development

Free medical coverage in HIP PPO

Retirement plan with high employer-con

Tuition reimbursement

FreeU education benefit

Job summary

Abbott is seeking a Field Clinical Specialist to work remotely covering Illinois for our Vascular division. The candidate must live or relocate to Illinois and undertake substantial travel.

The role involves overseeing clinical trials, coordinating protocol implementation, recruiting investigators, and ensuring safety reporting and regulatory compliance. Strong clinical research experience is essential.

Qualifications

• Associate's Degree
• 5+ years of relevant experience
• RN or RT with Cath Lab experience preferred
• Medical Device
• Clinical Trial and/or Research Experience

Responsibilities

• Oversee direction, planning, execution, clinical trials/research and data collection.
• Contributes to implementation of clinical protocols, and facilitates completion of final reports.
• Recruits clinical investigators and negotiates study design and costs.
• Direct human clinical trials, phases III & IV for company products under development.
• Participates in adverse event reporting and safety responsibilities monitoring.
• Coordinates and provides reporting information for reports submitted to the regulatory agencies.
• Monitors adherence to protocols by clinicians within a clinical setting.
• Monitors and determines study completion.
• Coordinates and oversees investigator initiations and group studies.
• May participate in adverse event reporting and safety responsibilities monitoring.
• May act as consultant/liaison with other corporations when working under licensing agreements.

Education

Associate's Degree

Job description

Abbott is seeking a Field Clinical Specialist to work remotely covering Illinois for our Vascular division. The candidate must live or relocate to Illinois and undertake substantial travel.

The role involves overseeing clinical trials, coordinating protocol implementation, recruiting investigators, and ensuring safety reporting and regulatory compliance. Strong clinical research experience is essential.