Manager, Clinical Education
About The Position
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries. 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.
Requirements
- 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.
- Knowledge of regulations and standards affecting IVDs (In Vitro Diagnostics) and Biologics.
- Has successfully led several high complexity projects.
Nice To Haves
- Medical Device/Diagnostics clinical experience is strongly preferred.
- Management experience in other clinical operations positions desirable.
- Certifications from the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) preferred.
Responsibilities
- Manages teams within 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
Benefits
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Manager
