Michael E. Morgan, Ph.D. Email & Phone Number
@cybin.com
1 phone found area 858
LinkedIn matched
Who is Michael E. Morgan, Ph.D.? Overview
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Michael E. Morgan, Ph.D. is listed as Sr. Director, DMPK at Helus Pharma, based in San Diego, California, United States. AeroLeads shows a work email signal at cybin.com, phone signal with area code 858, and a matched LinkedIn profile for Michael E. Morgan, Ph.D..
Michael E. Morgan, Ph.D. previously worked as Sr. Director DMPK at Cybin Inc. and DMPK CONSULTANT at Morgan Pharmaceutical Research. Michael E. Morgan, Ph.D. holds B.S., Microbiology And Biochemistry from Idaho State University.
Email format at Helus Pharma
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AeroLeads found 1 current-domain work email signal for Michael E. Morgan, Ph.D.. Compare company email patterns before reaching out.
About Michael E. Morgan, Ph.D.
I am personable, highly motivated and a self-titled science geek. Over 15+ years, I have obtained a comprehensive understanding of biopharmaceutical research and drug development. My principal strengths are DMPK analyses of preclinical and Phase 1 clinical modalities in multiple therapeutic areas. I have excellent oral communication and scientific writing skills. My backgrounds includes 60+ scientific meeting presentations, 40+ peer reviewed articles and 2+ patents. (see accomplishments)
Listed skills include Drug Development, Pharmacokinetics, Dmpk, Biotechnology, and 18 others.
Michael E. Morgan, Ph.D.'s current company
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Michael E. Morgan, Ph.D. work experience
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Sr. Director Dmpk
CurrentDmpk Consultant
Expertise: • Preclinical Pharmacokinetics• Toxicokinetics/Drug Safety• Clinical Pharmacokinetics• Pharmacokinetic modeling• Medical/Scientific Writing Clients:• Acadia Pharmaceuticals, Inc.• Arena Pharmaceuticals, Inc.• Beacon Discovery• Circumvent• Intercept Pharmaceuticals• LifeStar Pharma LLC• Outpost Medicine Limited
Director, Clinical Pharmacology
Senior Director, Pharmacokinetics
Led DMPK Discovery, Preclinical, Toxicology, and Clinical Programs.Member of the Senior Leadership Forum• Participated in 9+ programs that moved compounds forward to the next level of investigation• Coordinated, authored, and edited DMPK IND and NDA sections (4 INDs; 2 NDAs) for successful applications of 4+ new drug candidates• Analyzed, co-authored, and edited Clinical Study Reports (1 Phase 1a, 1 Phase 1b; 1 BE; 1 fed v. fasted) that resulted in FDA approval of the use of a new drug formulation for Belviq®• Modeled population pharmacokinetic and pharmacodynamic relationships that resulted in the scientific understanding of the drug response and drug concentration relationships
Director, Pharmacokinetics
Guided DMPK Discovery, Preclinical, Toxicology, and Clinical Programs• Participated in 5+ programs that moved compounds forward to the next level of investigation• Contributed to the analyses, coauthored, and edited the population PK and population PK/PD Phase 3 report that resulted in the FDA approval of Belviq®• Analyzed, co-authored, and edited preclinical PK and TK reports that moved compounds forward to the next level of investigation • Analyzed, co-authored, and edited Clinical Study Reports (5 Phase 1a, 5 Phase 1b; 2 Phase 3) that resulted in the FDA approval of Belviq®
Associate Director
Built strong scientific DMPK portfolios for advancing drug candidates• Participated in 9+ programs that moved compounds forward to the next level of investigation• Initiated and completed 21CRF Part 11 compliance for WinNonlin that resulted GLP compliant PK and TK analyses • Analyzed, authored, and edited preclinical PK, TK and Clinical Studies Reports that moved compounds forward to the next level of investigation
Senior Scientist
Built strong scientific DMPK portfolios for advancing drug candidates• Participated in 9+ programs that moved compounds forward to the next level of investigation• Instituted one-page PK data summaries that resulted in improved communication with the project teams• Analyzed, authored, and edited preclinical PK and TK reports that moved compounds forward to the next level of investigation
Scientist
Established scientific rigor within the PK team• Participated in 9+ programs that moved compounds forward to next level of investigation• Designed protocols for PK in-life experiments and developed new procedures that resulted in an 50% increase in the number of animal experiments performed
Michael E. Morgan, Ph.D. education
B.S., Microbiology And Biochemistry
Ph.D., Pharmacology
Postdoctoral Fellow, Clinical Pharmacology
Frequently asked questions about Michael E. Morgan, Ph.D.
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What company does Michael E. Morgan, Ph.D. work for?
Michael E. Morgan, Ph.D. works for Helus Pharma.
What is Michael E. Morgan, Ph.D.'s role at Helus Pharma?
Michael E. Morgan, Ph.D. is listed as Sr. Director, DMPK at Helus Pharma.
What is Michael E. Morgan, Ph.D.'s email address?
AeroLeads has found 1 work email signal at @cybin.com for Michael E. Morgan, Ph.D. at Helus Pharma.
What is Michael E. Morgan, Ph.D.'s phone number?
AeroLeads has found 1 phone signal(s) with area code 858 for Michael E. Morgan, Ph.D. at Helus Pharma.
Where is Michael E. Morgan, Ph.D. based?
Michael E. Morgan, Ph.D. is based in San Diego, California, United States while working with Helus Pharma.
What companies has Michael E. Morgan, Ph.D. worked for?
Michael E. Morgan, Ph.D. has worked for Helus Pharma, Cybin Inc., Morgan Pharmaceutical Research, Mirati Therapeutics, and Arena Pharmaceuticals.
How can I contact Michael E. Morgan, Ph.D.?
You can use AeroLeads to view verified contact signals for Michael E. Morgan, Ph.D. at Helus Pharma, including work email, phone, and LinkedIn data when available.
What schools did Michael E. Morgan, Ph.D. attend?
Michael E. Morgan, Ph.D. holds B.S., Microbiology And Biochemistry from Idaho State University.
What skills is Michael E. Morgan, Ph.D. known for?
Michael E. Morgan, Ph.D. is listed with skills including Drug Development, Pharmacokinetics, Dmpk, Biotechnology, Pharmacology, Ind, Clinical Development, and In Vitro.
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