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Debie Hoivik
Debie Hoivik
Medicine Safety Evaluation | Akebia Therapeutics
Massachusetts, Cambridge, United States
Debie Hoivik
Summary
Debie Hoivik is an accomplished leader with over 20 years of experience in nonclinical drug safety and translational medicine. Currently serving as Vice President of Early Development at Akebia Therapeutics, Debie has a proven track record in overseeing nonclinical safety assessments for therapeutic candidates aimed at improving patient outcomes in kidney disease. Her extensive background includes significant roles at major pharmaceutical companies such as GSK and Boehringer Ingelheim, where she managed diverse operations and led strategic global projects. With a Ph.D. in Pharmacology and Toxicology from the University of Connecticut, Debie combines scientific expertise with strong leadership skills. Her interests lie in operational excellence and compliance within the pharmaceutical industry, making her a key asset in any organization focused on drug development and safety. Debie is also known for her adaptability in navigating complex regulatory environments and fostering collaboration across multidisciplinary teams.
Debie Hoivik
Work Experience
Vice President, Early Development at
Akebia Therapeutics
February 2022 - Present
Debie Hoivik
Education
University of Connecticut, Doctor of Philosophy (Ph.D.), Pharmacology and Toxicology
Texas A&M University, Post-Doc
Frequently Asked Questions about Debie Hoivik
What is Debie Hoivik email address?
Debie Hoivik's primary email address is ************@boehringer-ingelheim.com. To view the full verified email and additional contact details, sign up for free with Muraena.
What company does Debie Hoivik work for?
Debie Hoivik is a Medicine Safety Evaluation at Akebia Therapeutics.
Where Debie Hoivik graduated from?
Debie Hoivik holds a degree in null from University of Connecticut.
How can I directly contact Debie Hoivik?
To contact Debie Hoivik directly, you can use the email address ************@boehringer-ingelheim.com. Complete contact information is available upon registration with Muraena.
Who is Debie Hoivik?
Debie Hoivik is an accomplished leader with over 20 years of experience in nonclinical drug safety and translational medicine. Currently serving as Vice President of Early Development at Akebia Therapeutics, Debie has a proven track record in overseeing nonclinical safety assessments for therapeutic candidates aimed at improving patient outcomes in kidney disease. Her extensive background includes significant roles at major pharmaceutical companies such as GSK and Boehringer Ingelheim, where she managed diverse operations and led strategic global projects. With a Ph.D. in Pharmacology and Toxicology from the University of Connecticut, Debie combines scientific expertise with strong leadership skills. Her interests lie in operational excellence and compliance within the pharmaceutical industry, making her a key asset in any organization focused on drug development and safety. Debie is also known for her adaptability in navigating complex regulatory environments and fostering collaboration across multidisciplinary teams.
Debie`s contact details
************@boehringer-ingelheim.com
*********@sprintmail.com
*******@akebia.com
Colleagues
Group Vice President
Senior Product Trainer | Health Systems Manager | Government Account Manager | Sales Representative
Volunteer
Cost Accountant
Print Billing Coordinator/Senior Billing Coordinator
Chief Of Staff
Sales Representative
Resident in Internal Medicine
Summer Intern
Medical Information Associate