Sarah Hubbard

Sarah Hubbard Email and Phone Number

Clinical Program & Asset Development Leader @ Regeneron
Sarah Hubbard's Location
London, England, United Kingdom, United Kingdom
Sarah Hubbard's Contact Details

Sarah Hubbard personal email

About Sarah Hubbard

Dynamic R&D Strategy and clinical operations professional with extensive experience in asset, program and trial management for the Pharmaceutical & Biotech industry. Demonstrated ability to lead cross-functional teams in a fast paced and constantly evolving environment. Ability to think flexibly and adapt operational approach to each disease area/ asset when required. Strong experience in whole aspect of drug development and management, from pre-clinical through to post-marketing/ medical affairs including device development.

Sarah Hubbard's Current Company Details
Regeneron

Regeneron

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Clinical Program & Asset Development Leader
Sarah Hubbard Work Experience Details
  • Regeneron
    Program Operations Lead (Pol) Director
    Regeneron Oct 2023 - Present
    Tarrytown, New York, Us
    Part of leadership team within Regeneron's newly formed Genetic Medicines group. Leading high performing teams in the delivery of genetic therapies, using cutting edge technologies in the treatment of ALS, hemophilia, and other rare disease.
  • Biogen
    Clinical Operations Program Lead (Copl) & R&D Project Lead (Rdpl)
    Biogen May 2021 - Sep 2023
    Cambridge, Ma, Us
    I had a dual role at Biogen as both a clinical operations program manager and an R&D project lead. As a R&D project lead, I was accountability for an early phase ASO asset for the treatment of a rare paediatric orphan disease. The R&D Project lead role meant I was the central point of accountability for the R&D project team, a high performing team of senior cross-functional representatives. This includes Commerical, Asset Management, Biostats, Clinical Pharmacology/ Toxicology as well as operations. My role was a strategic role, lead the team in preparation of governance and regulatory interactions, and asset progression. In my role as the operations program lead, I was accountability for the operational success of studies conducted to deliver the clinical development plan (CDP). I also sat at the R&D project team table as the operations representative. Through both of these roles, I had a keen vantage point on drug development- all the way from pre-clinical through to post-marketing. My role also involved direct involvement in interaction with external stakeholders, including advocacy groups and research partners. I was frequently asked to participate in alliance strategic meetings and to provide input into commercial activities such as press releases and business development, etc. I was been incredibly proud and grateful to lead a team that pioneered Biogen's first fully remote study, which has gained industry -wide recognition at the US Reuters Pharma awards in 2022, where we were joint runners up for the Inclusive Trials award. Key words: Genetic neuro degenerative disease, rare genetic disease, ASO development. Angelman Syndrome, Aicardi Goutieres Syndrome (AGS), Paediatrics, Pediatrics, KCNT1 epilepsy, governance, alliance, early phase
  • Biogen
    Associate Director Clinical Operations
    Biogen Mar 2015 - Apr 2021
    Cambridge, Ma, Us
  • Astellas Pharma Europe
    Late Phase/ Medical Affairs Operations Manager
    Astellas Pharma Europe Oct 2013 - Mar 2015
    Associate Director, Late Phase Clinical Development & Operations, Medical Affairs Europe
  • Amgen
    Clinical Programme Operations Manager
    Amgen Oct 2011 - Oct 2013
    Thousand Oaks, Ca, Us
    Senior Manager (CPOM) overseeing high priority, pivotal International Phase II & Phase III programme.
  • Amgen
    Clinical Research Study Manager
    Amgen Jan 2005 - Oct 2011
    Thousand Oaks, Ca, Us
    Clinical Study Manager: European & International Phase III & IV interventional and non-interventional studies.
  • Gsk
    Clinical Study Manager (Contract)
    Gsk 2004 - 2005
    Brentford, Middlesex, Gb
    European Study Management
  • Wyeth
    Principle Cra
    Wyeth 2003 - 2004
    New York, New York, Us
  • Pra International
    Scra/ Project Manager
    Pra International 2001 - 2002
    Raleigh, North Carolina, Us
    Local study manager - Sydney, Australia
  • Novartis
    Lead Cra
    Novartis 2000 - 2001
    Basel, Baselstadt, Ch
  • Mds Pharma Services
    Senior Cra
    Mds Pharma Services 1998 - 2000
    King Of Prussia, Pennsylvania, Us
    Partly based in Phoeniz, AZ, USA
  • Quintiles
    Cra
    Quintiles 1997 - 1998
    Durham, North Carolina, Us
  • Innovex
    Cra, Pharm Officer (Contracted)
    Innovex 1996 - 1998
    Us
  • Novo Nordisk A/S
    Cra
    Novo Nordisk A/S 1996 - 1997
    Bagsværd, Dk
  • Merck Sharp & Dohme
    Pharmacovigillance Officer
    Merck Sharp & Dohme 1996 - 1997
    Rahway, New Jersey, Us
  • Gsk
    Assistant Scientist
    Gsk Aug 1994 - Aug 1995
    Brentford, Middlesex, Gb

Sarah Hubbard Skills

Clinical Trials Clinical Development Biotechnology Clinical Research Pharmaceutical Industry Gcp Cro Clinical Study Design Clinical Research Associates Ctms Oncology Pharmaceutics Ich Gcp Drug Development Clinical Monitoring Edc Lifesciences Regulatory Submissions Sop Pharmacovigilance Life Sciences

Sarah Hubbard Education Details

  • King'S College London
    King'S College London
    Pharmacology

Frequently Asked Questions about Sarah Hubbard

What company does Sarah Hubbard work for?

Sarah Hubbard works for Regeneron

What is Sarah Hubbard's role at the current company?

Sarah Hubbard's current role is Clinical Program & Asset Development Leader.

What is Sarah Hubbard's email address?

Sarah Hubbard's email address is hu****@****ail.com

What schools did Sarah Hubbard attend?

Sarah Hubbard attended King's College London.

What skills is Sarah Hubbard known for?

Sarah Hubbard has skills like Clinical Trials, Clinical Development, Biotechnology, Clinical Research, Pharmaceutical Industry, Gcp, Cro, Clinical Study Design, Clinical Research Associates, Ctms, Oncology, Pharmaceutics.

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