Mark Holbrook

Mark Holbrook Email and Phone Number

Pharma Consultant: specialising in non-clinical pharmacology and drug safety @
Mark Holbrook's Location
Harrogate, England, United Kingdom, United Kingdom
Mark Holbrook's Contact Details

Mark Holbrook personal email

About Mark Holbrook

Mark Holbrook is a Pharma Consultant: specialising in non-clinical pharmacology and drug safety at VAST pharma solutions. He possess expertise in safety pharmacology, glp, pharmaceutical industry, pharmacology, drug discovery and 36 more skills.

Mark Holbrook's Current Company Details
VAST pharma solutions

Vast Pharma Solutions

Pharma Consultant: specialising in non-clinical pharmacology and drug safety
Mark Holbrook Work Experience Details
  • Vast Pharma Solutions
    Co-Founder, Director
    Vast Pharma Solutions Apr 2016 - Present
    Harrogate, United Kingdom
    We provide Value Added Science & Technology (VAST) solutions to the pharma industry to support drug discovery and early development projects, programmes and portfolios. Since every molecule and project is different we work to…identify the question and design the right experiment to address this, at the right time in the most efficient way and so aid more informed decision making.Our VAST experience has been gained from >25 years working in small, mid and large pharma and the CRO industry. We have led and supported projects from target identification to regulatory filing with specialist expertise in non-clinical pharmacology and safety pharmacology/drug safety.
  • Covance
    Vice President, Head Of Science Early Development & Head Global Safety Pharmacology
    Covance Aug 2014 - Mar 2016
    • Leadership of the science strategy for Early Development which includes all non-clinical work from lead optimization to clinic• Leadership of the scientific, strategic and business development of safety pharmacology across 5 sites in Eu, US and Asia. Includes core battery, novel discovery support/mechanistic capabilities, integration into DMPK and toxicology studies and clinical translation.• Leadership of the development of a new business capability; Early Phase Development Solutions (EPDS) from concept to launch. EPDS is a drug development capability comprising all the non-clinical, clinical and regulatory capabilities from LO to clinical POC
  • Covance
    Vice President, Global Science Lead Safety Pharmacology & Site Lead Safety Assessment
    Covance Jan 2012 - Jul 2013
    Harrogate, United Kingdom
  • Pfizer
    Executive Director, Head Global Safety Pharmacology
    Pfizer 1999 - Jan 2012
    Sandwich, Uk
  • Astrazeneca
    Team Leader, Discovery
    Astrazeneca Jan 1995 - Aug 1999
  • Celltech
    Team Leader
    Celltech Nov 1990 - Jun 1995
    Slough, United Kingdom

Mark Holbrook Skills

Safety Pharmacology Glp Pharmaceutical Industry Pharmacology Drug Discovery Toxicology Clinical Trials Regulatory Affairs Cro Clinical Development Regulatory Submissions Drug Development Leadership Lifesciences Pharmaceutics Biotechnology Ind Biochemistry Biomarkers R&d Oncology Immunology Fda Biopharmaceuticals Clinical Research In Vivo Gcp Cross Functional Team Leadership In Vitro Sop Vaccines Infectious Diseases Clinical Pharmacology Pharmacovigilance Medical Writing Life Sciences Cro Management Good Laboratory Practice Standard Operating Procedure Research And Development Good Clinical Practice

Mark Holbrook Education Details

Frequently Asked Questions about Mark Holbrook

What company does Mark Holbrook work for?

Mark Holbrook works for Vast Pharma Solutions

What is Mark Holbrook's role at the current company?

Mark Holbrook's current role is Pharma Consultant: specialising in non-clinical pharmacology and drug safety.

What is Mark Holbrook's email address?

Mark Holbrook's email address is ma****@****ail.com

What schools did Mark Holbrook attend?

Mark Holbrook attended University Of Liverpool, Brierton Comprehensive.

What skills is Mark Holbrook known for?

Mark Holbrook has skills like Safety Pharmacology, Glp, Pharmaceutical Industry, Pharmacology, Drug Discovery, Toxicology, Clinical Trials, Regulatory Affairs, Cro, Clinical Development, Regulatory Submissions, Drug Development.

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