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@abbvie.com
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Meg Drew is listed as Pharmaceutical Regulatory Affairs and Portfolio Program Management Professional at AbbVie, a with 46234 employees, based in North Chicago, Illinois, United States. AeroLeads shows a work email signal at abbvie.com, phone signal with area code 847, and a matched LinkedIn profile for Meg Drew.
Meg Drew previously worked as DIRECTOR, Portfolio Program Management - Specialty Products at Abbvie and SCIENTIFIC DIRECTOR, US Medical Affairs - Dermatology at Abbvie. Meg Drew holds Bs from University Of Illinois Urbana-Champaign.
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AeroLeads found 1 current-domain work email signal for Meg Drew. Compare company email patterns before reaching out.
Meg Drew is a Pharmaceutical Regulatory Affairs and Portfolio Program Management Professional at AbbVie. She possess expertise in clinical trials, immunology, regulatory strategy, regulatory submissions, regulatory affairs and 16 more skills.
Listed skills include Clinical Trials, Immunology, Regulatory Strategy, Regulatory Submissions, and 17 others.
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Co-Leads Asset Strategy Teams to ensure seamless translation of asset strategy into integrated execution plans, leading to improvement in team effectiveness and alignment. Accountable for management of more than 10 assets spanning complete drug development life cycle and on-market optimization.
Leveraged extensive regulatory knowledge within new role to become well-rounded leader with experience in data generation, functional planning and developing scientific communication materials related to hidradenitis suppurativa and atopic dermatitis.
Accomplished Global Regulatory Lead for immunology digital health program, upadacitinib (JAK inhibitor) for giant cell arteritis and atopic dermatitis as well as risankizumab (anti-IL-23) for atopic dermatitis and hidradenitis suppurativa. Instituted PharmD externship program in partnership with Purdue University within AbbVie Regulatory.
• Managed the development of, and execution against, a global regulatory strategy for Inositol forRetinopathy of Prematurity. • Led a cross-divisional initiative to develop a long-term regulatory systems/IT strategy.• Chaired departmental business leadership development initiative.
• Established a framework for the effective and efficient management of all regulatory operational support required by newly created established pharmaceuticals division within Abbott and acted as change agent to ensure business continuity during implementation of the new department structure.• Led EPD RA in Business Separation Project activities to allow for divestiture of the Proprietary Pharmaceuticals Division (now AbbVie) from Abbott. Received Abbott Transition Office Award for Business Separation Project (Abbott/AbbVie).• Managed functional budget in excess of $35MM with 5 direct reports and 100+ indirect reports across three countries and four sites.
• Provided leadership and expertise in the management of processes and timelines for major US and EU submissions and projects, including cross-functional projects.• Responsible for strategically prioritizing resources across project portfolio.• Regulatory Affairs Project Management Lead for Solvay Integration.
• Global Regulatory Lead for Humira new indications, including Crohn’s Disease indication approvals in United States (US), European Union (EU) and other first-wave submission countries.• Led team preparation for and facilitated nine key agency meetings within a ten-month period.
Other employees you can reach at abbvie.com. View company contacts for 46234 employees →
Clauber Reis
Colleague at AbbvieSão Paulo, Brazil
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Susan Basinger
Colleague at AbbvieWaukegan, Illinois, United States
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Robin Bakaj
Colleague at AbbvieGreater Chicago Area, United States
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Kabir Khattabi
Colleague at AbbvieMontreal, Quebec, Canada
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Anjla Sood
Colleague at AbbvieUnited States
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Elizabeth Condie
Colleague at AbbvieScottsdale, Arizona, United States
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Nizar Moneer
Colleague at AbbvieSanta Rosa, California, United States
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Dung Dong
Colleague at AbbvieHo Chi Minh City, Vietnam, Viet Nam
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Megan Walsh
Colleague at AbbvieGreater Boston, United States
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Steve Bath
Colleague at AbbvieLincoln, Nebraska, United States
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Quick answers generated from the profile data available on this page.
Meg Drew works for AbbVie.
Meg Drew is listed as Pharmaceutical Regulatory Affairs and Portfolio Program Management Professional at AbbVie.
AeroLeads has found 1 work email signal at @abbvie.com for Meg Drew at AbbVie.
AeroLeads has found 1 phone signal(s) with area code 847 for Meg Drew at AbbVie.
Meg Drew is based in North Chicago, Illinois, United States while working with AbbVie.
Meg Drew has worked for Abbvie, Abbott, and Abbott Laboratories.
Meg Drew's colleagues at AbbVie include Clauber Reis, Susan Basinger, Robin Bakaj, Kabir Khattabi, and Anjla Sood.
You can use AeroLeads to view verified contact signals for Meg Drew at AbbVie, including work email, phone, and LinkedIn data when available.
Meg Drew holds Bs from University Of Illinois Urbana-Champaign.
Meg Drew is listed with skills including Clinical Trials, Immunology, Regulatory Strategy, Regulatory Submissions, Regulatory Affairs, Regulatory Operations, Quality Systems, and Registration Management.
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