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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 114,000 colleagues serve people in more than 160 countries.

The Opportunity:

Our location in Alameda, California has an opportunity for an experienced professional in the Medical Affairs Sub-Function, who possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.

What you will do:

•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.

_Requirements:_

Must have an Associate's Degree in a relatable field of study

0-2 years of experience in a similar role.

The base pay for this position is $68,700.00 – $105,300.00. In specific locations, the pay range may vary from the range posted.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email [email protected]