Manager, Clinical Education

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:

• Career development with an international company where you can grow the career of which you dream.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

We are seeking a Clinical Education Manager for our Vascular division. This is a fully REMOTE role.  

Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents

Manages teams within the Medical Affairs Sub-Function.

Focus is on policy and strategy implementation and control rather than development.

Typically handles short-term operational/tactical responsibilities.

Core Job Responsibilities

• As the Manager of the Medical Affairs Sub-Function, oversees the strategy implementation and operations for overseeing the direction, planning, execution, clinical trials/research and the data collection activities.
• Contributes to implementation of clinical protocols, and facilitates completion of final reports.
• Recruits clinical investigators and negotiates study design and costs.
• Responsible for directing 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 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 and Experience you’ll bring

• Bachelor's degree, discipline appropriate to the project environment, clinical research, scientific and technical degree is preferred.
• 5 years of related work experience with a good understanding of specified functional area, or Master's degree with 3 years of related work experience.
• Experience as a CRA, direct clinical research experience, or an equivalent combination of education and work experience.  Medical Device/Diagnostics clinical experience is strongly preferred. Management experience in other clinical operations positions desirable.
• Knowledge of regulations and standards affecting IVDs (In Vitro Diagnostics) and Biologics.
• Has successfully led several high complexity projects.
• Certifications from the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) preferred.

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