Michelle Parker Abraham Email & Phone Number | Management Professional with over 15 years of experience within Regulatory and Clinical Affairs focusing on regulatory submissions, protocol development and supervising clinical affairs teams by utilizing strategic, hands on leadership. Extensive expertise in Regulatory Affairs, Clinical Research, and Project Management. Leads clinical and scientific translation of research and development, for new medical devices. Coaches and trains employees to achieve organizational objectives, while maximizing productivity and efficiency. Previous positions held include Regulatory Affairs Manager, Senior Regulatory Specialist, and Senior Clinical Research Associate. Highlights of Expertise: • 510(k) Submissions • FDA Clearance • Protocol Development • Medical Devices • Product Registration • Technical Guidance • Relationship Development Diverse background in different functional groups, along with participation in the publication of numerous research studies, leads to the application of innovative solutions to resolve urgent challenges. A track record of overall success has left a lasting impact on organizations.

Michelle Parker Abraham

Management Professional with over 15 years of experience within Regulatory and Clinical Affairs focu...
Chicago, Chicago, United States

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Michelle Parker Abraham’s Email abrahamm@sysmex.com

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Michelle Parker Abraham’s Location Chicago, Chicago, United States

Michelle Parker Abraham’s Current Industry Abbott

Michelle Parker Abraham’s Prior Industry Baebies | Sysmex America | Abbott Laboratories | Northwestern Memorial Hospital

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Director of Regulatory Affairs

2023-09-01 00:00:00 - Present

Director Regulatory and Clinical Affairs

2020-04-01 00:00:00 - 2021-08-01 00:00:00

Manager Regulatory Affairs

2017-03-01 00:00:00 - 2020-04-01 00:00:00

Senior Clinical Research Associate

2007-10-01 00:00:00 - 2013-07-01 00:00:00

Medical Technologist

2006-06-01 00:00:00 - 2007-10-01 00:00:00

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Michelle Parker Abraham is a Management Professional with over 15 years of experience within Regulatory and Clinical Affairs focusing on regulatory submissions, protocol development and supervising clinical affairs teams by utilizing strategic, hands on leadership. Extensive expertise in Regulatory Affairs, Clinical Research, and Project Management. Leads clinical and scientific translation of research and development, for new medical devices. Coaches and trains employees to achieve organizational objectives, while maximizing productivity and efficiency. Previous positions held include Regulatory Affairs Manager, Senior Regulatory Specialist, and Senior Clinical Research Associate. Highlights of Expertise: • 510(k) Submissions • FDA Clearance • Protocol Development • Medical Devices • Product Registration • Technical Guidance • Relationship Development Diverse background in different functional groups, along with participation in the publication of numerous research studies, leads to the application of innovative solutions to resolve urgent challenges. A track record of overall success has left a lasting impact on organizations.

Michelle Parker Abraham has prior
experience in the following industries:
Baebies | Sysmex America | Abbott Laboratories | Northwestern Memorial Hospital

Michelle Parker Abraham has the following professional experience:
Abbott | Baebies | Sysmex America | Abbott Laboratories | Northwestern Memorial Hospital