Clinical Research Associate

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

Working at Abbott

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 you dream of.
• 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.

The Opportunity

This position works out remote in the Diagnostics Division.

We’re empowering smarter medical and economic decision making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people. We are seeking an experienced professional individual contributor to join our team. This role operates under limited supervision and requires the application of subject matter knowledge in Medical Affairs.

What You’ll Work On

As an experienced professional in the Medical Affairs Sub-Function, you will:

• Oversee the direction, planning, execution, and data collection activities of clinical trials/research.
• Contribute to the implementation of clinical protocols and facilitate the completion of final reports.
• Recruit clinical investigators and negotiate study design and costs.
• Direct human clinical trials (phases III & IV) for company products under development.
• Participate in adverse event reporting and safety monitoring.
• Coordinate and provide information for reports submitted to regulatory agencies.
• Monitor adherence to protocols and determine study completion.
• Coordinate and oversee investigator-initiated and group studies.
• Act as a consultant/liaison with other corporations under licensing agreements.
• Apply skills and knowledge to meet specific needs and requirements.
• Work independently while contributing to team goals.