Fedra Molaie-Holagh
Experienced senior regulatory affairs professional with a demonstrated history of working in the pharmaceuticals and biotech industry as... | Mississauga, Ontario, Canada
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Fedra Molaie-Holagh’s Emails fm****@to****.com
Fedra Molaie-Holagh’s Phone Numbers No phone number available.
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Fedra Molaie-Holagh’s Location Mississauga, Ontario, Canada
Fedra Molaie-Holagh’s Expertise Experienced senior regulatory affairs professional with a demonstrated history of working in the pharmaceuticals and biotech industry as well provide support as a senior strategic consultant. Skilled in U.S. Food and Drug Administration (FDA), Health Canada requirements and strategies for registering products stewardship throughout life cycle management. Strong scientific affairs professional with 20 years of experience in the pharmaceutical industry, focusing in global regulatory affairs. Demonstrated strategic and analytical skills to support determining best approval pathways and ensuring successful interactions with health authorities with the highest potential for positive outcomes. I’ve led teams as director/ head of the regulatory department managing development of investigational products through marketing application submission/approval including post-approval lifecycle management and product stewardship. Therapeutic area experience consists of oncology, nephrology, analgesia, as well as men’s health. Experienced with biologics, NCE and small molecules as well as cannabis.
Fedra Molaie-Holagh’s Current Industry Premier Consulting
Fedra
Molaie-Holagh’s Prior Industry
University Of Toronto
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Visible Genetics
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Amgen
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Ym Biosciences
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Novartis Animal Health
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Bgp Pharma
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Acerus Pharma
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Regulatory Professionals
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Regulatory Professionals A Division Of Premier Research
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Premier Consulting
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Work Experience
Premier Consulting
Vice President Regulatory Affairs
Mon Apr 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Premier Consulting
Senior Director Regulatory Affairs
Tue Feb 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Apr 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time)
Regulatory Professionals A Division Of Premier Research
Senior Director of Regulatory Affairs
Sat Jan 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Mar 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)
Regulatory Professionals
Director of Regulatory Affairs
Sun Nov 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Dec 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Acerus Pharma
Director Regulatory Affairs
Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Nov 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time)
Bgp Pharma
Manager Regulatory Affairs
Mon Feb 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Dec 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Amgen
Manager, Regulatory Affairs
Fri May 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Feb 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis Animal Health
Head of Regulatory Affairs - Canada
Tue Jul 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Apr 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis Animal Health
Head (acting), Regulatory Affairs
Thu May 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Jul 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis Animal Health
Associate Director Regulatory Affairs
Sat Jun 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Jul 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis Animal Health
Senior Manager, Regulatory Affairs
Sat Sep 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Jun 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)
Ym Biosciences
Senior Manager, Regulatory Affairs
Mon Jan 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Aug 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
Amgen
Senior Associate, Regulatory Affairs
Tue Jan 01 2002 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2006 00:00:00 GMT+0000 (Coordinated Universal Time)
Visible Genetics
QA/QC Associate
Sat Jan 01 2000 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Jan 01 2002 00:00:00 GMT+0000 (Coordinated Universal Time)
University Of Toronto
Teaching Assistant (Undergraduate - Laboratory)
Sun Jan 01 1995 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jan 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Fedra Molaie-Holagh Email Addresses
FAQ About Fedra Molaie-Holagh
-
Fedra Molaie-Holagh is located at
Mississauga, Ontario, Canada -
Fedra Molaie-Holagh is a
Experienced senior regulatory affairs professional with a demonstrated history of working in the pharmaceuticals and biotech industry as well provide support as a senior strategic consultant. Skilled in U.S. Food and Drug Administration (FDA), Health Canada requirements and strategies for registering products stewardship throughout life cycle management. Strong scientific affairs professional with 20 years of experience in the pharmaceutical industry, focusing in global regulatory affairs. Demonstrated strategic and analytical skills to support determining best approval pathways and ensuring successful interactions with health authorities with the highest potential for positive outcomes. I’ve led teams as director/ head of the regulatory department managing development of investigational products through marketing application submission/approval including post-approval lifecycle management and product stewardship. Therapeutic area experience consists of oncology, nephrology, analgesia, as well as men’s health. Experienced with biologics, NCE and small molecules as well as cannabis. Premier Consulting -
Fedra Molaie-Holagh currently works in the
Premier Consulting -
Fedra Molaie-Holagh specializes in
Experienced senior regulatory affairs professional with a demonstrated history of working in the pharmaceuticals and biotech industry as well provide support as a senior strategic consultant. Skilled in U.S. Food and Drug Administration (FDA), Health Canada requirements and strategies for registering products stewardship throughout life cycle management. Strong scientific affairs professional with 20 years of experience in the pharmaceutical industry, focusing in global regulatory affairs. Demonstrated strategic and analytical skills to support determining best approval pathways and ensuring successful interactions with health authorities with the highest potential for positive outcomes. I’ve led teams as director/ head of the regulatory department managing development of investigational products through marketing application submission/approval including post-approval lifecycle management and product stewardship. Therapeutic area experience consists of oncology, nephrology, analgesia, as well as men’s health. Experienced with biologics, NCE and small molecules as well as cannabis. -
Fedra Molaie-Holagh speaks the following languages:
No languages available. -
Fedra Molaie-Holagh has prior experience in the following industries:
Premier Consulting , Regulatory Professionals A Division Of Premier Research , Regulatory Professionals , Acerus Pharma , Bgp Pharma , Amgen , Novartis Animal Health , Novartis Animal Health , Novartis Animal Health , Novartis Animal Health , Ym Biosciences , Amgen , Visible Genetics , University Of Toronto -
Fedra Molaie-Holagh has the following professional experience:
Premier Consulting , Premier Consulting , Regulatory Professionals A Division Of Premier Research , Regulatory Professionals , Acerus Pharma , Bgp Pharma , Amgen , Novartis Animal Health , Novartis Animal Health , Novartis Animal Health , Novartis Animal Health , Ym Biosciences , Amgen , Visible Genetics , University Of Toronto . -
You can view Fedra Molaie-Holagh’s
LinkedIn profile at LinkedIn URL. -
Fedra Molaie-Holagh’s work email addresses are
[email protected] . -
Fedra Molaie-Holagh works at
Premier Consulting
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