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Heidi Colton

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Heidi Colton

Executive Director, Nonclinical Development Strategy and Translational Medicine | Chimerix, Inc.

Apex, North Carolina, United States

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Heidi Colton

Summary

Heidi Colton is an accomplished Executive Director with extensive experience in the pharmaceutical and biotechnology sectors, specializing in nonclinical and translational development strategies. Her career spans both big pharma and small biotech environments, where she has successfully led initiatives in antiviral, antibacterial, and oncology drug development. Heidi's expertise lies in designing translational medicine strategies and managing complex regulatory submissions, having independently delivered multiple nonclinical IND/NDA packages. She possesses strong leadership skills, having effectively guided international matrix teams towards achieving project goals. With a solid background in toxicology and pharmacovigilance, she is well-versed in clinical safety and risk management. Heidi is also recognized for her regulatory writing proficiency and has a hands-on laboratory experience that enhances her strategic insights. Her educational foundation includes a BS in Microbiology from Penn State University and further studies at North Carolina State University. Outside of her professional endeavors, Heidi is passionate about advancing the field of drug development through innovative biomarker strategies.

General

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Technical Background

Leadership Experience

Long-Term Tenure

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Emerging Technologies

Leadership Development

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Corporate Experience

Heidi Colton

Work Experience

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Executive Director, Nonclinical Development Strategy and Translational Medicine at

Chimerix, Inc.

January 2023 - Present

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Executive Director, Toxicology & Translational Medicine at

Chimerix, Inc.

January 2021 - January 2023

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Senior Director, Toxicology & Translational Medicine at

Chimerix, Inc.

January 2019 - January 2021

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Director, Toxicology at

Chimerix, Inc.

December 2015 - January 2019

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Associate Director, Toxicology at

Chimerix, Inc.

April 2015 - December 2015

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Director, Investigative Toxicology at

GSK

January 2014 - April 2015

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Clinical Safety Scientist - Global Clinical Safety and Pharmacovigilance at

GSK

January 2013 - September 2013

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Senior Scientific Investigator- Nonclinical Safety Assessment at

GSK

January 2002 - January 2009

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Scientist - Toxicogenomics- Nonclinical Safety Assessment at

GSK

January 2001 - January 2002

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Associate Scientist- Microbiology, Pharmaceutical Development at

GSK

January 1996 - January 2001

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Heidi Colton

Education

North Carolina State University

January 2000 - January 2002

Penn State University, Bs

January 1992 - January 1996

Frequently Asked Questions about Heidi Colton

What is Heidi Colton email address?

Heidi Colton's primary email address is *******@chimerix.com. To view the full verified email and additional contact details, sign up for free with Muraena.

What company does Heidi Colton work for?

Heidi Colton is a Executive Director, Nonclinical Development Strategy and Translational Medicine at Chimerix, Inc., a company specializing in Commercial physical research.

Where Heidi Colton graduated from?

Heidi Colton holds a degree in from North Carolina State University.

How can I directly contact Heidi Colton?

To contact Heidi Colton directly, you can use the email address *******@chimerix.com. Complete contact information is available upon registration with Muraena.

Who is Heidi Colton?

Heidi Colton is an accomplished Executive Director with extensive experience in the pharmaceutical and biotechnology sectors, specializing in nonclinical and translational development strategies. Her career spans both big pharma and small biotech environments, where she has successfully led initiatives in antiviral, antibacterial, and oncology drug development. Heidi's expertise lies in designing translational medicine strategies and managing complex regulatory submissions, having independently delivered multiple nonclinical IND/NDA packages. She possesses strong leadership skills, having effectively guided international matrix teams towards achieving project goals. With a solid background in toxicology and pharmacovigilance, she is well-versed in clinical safety and risk management. Heidi is also recognized for her regulatory writing proficiency and has a hands-on laboratory experience that enhances her strategic insights. Her educational foundation includes a BS in Microbiology from Penn State University and further studies at North Carolina State University. Outside of her professional endeavors, Heidi is passionate about advancing the field of drug development through innovative biomarker strategies.

Heidi`s contact details

mail

*******@chimerix.com

**************@gsk.com

Colleagues

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Norlonn Sturdivant Mt Rac

Executive Director of Quality Assurance

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Tom Brundage

Vice President, Biostatistics

Mike Sherman

Member Board of Directors

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Joshua Allen

Chief Scientific Officer

Barbara Berg

Executive Director, Human Resources

Christopher Jordan

Vice President Regulatory Affairs

Odin Naderer

VP Clinical Pharmacology/Translational Medicine

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