Experience

Ethos Pharmaceutical Ethics & Compliance

• United Kingdom
• Professional Training and Coaching
• 1 - 100 Employee

• Founding Partner Ethos Pharmaceutical Ethics and Compliance

  • Jun 2019 - Present



Makara Health Communications

• United Kingdom
• Advertising Services
• 1 - 100 Employee

• Specialist consultant and educator in pharmaceutical ethics and compliance

  • Mar 2017 - Present



Green Bear Medical

• Director

  • 2013 - Present



Havas Lynx Group

• United Kingdom
• Advertising Services
• 300 - 400 Employee

• Medical Director

  • Jul 2013 - Aug 2015

  I led and developed the medical capability of Havas Lynx in provision of medical education. We facilitated scientific exchange between medical departments and the physicians they interact with and developed creative digital techniques to communicate complex medical information in memorable and comprehensible ways.



Broughtonwalker Medical Limited

• United Kingdom
• Pharmaceutical Manufacturing

• Director

  • Jan 2008 - Jun 2013

  As a consultant in pharmaceutical medicine I worked for a variety of large and medium-sized companies. The roles included medical director at UK and European level leading medical teams, global medical advisory roles and a role in a major clinical research programme.In addition I provided training in compliance with UK and European Codes of Practice to medical and commercial teams within pharma.



Independent pharmaceutical consutant

• Director Pharmaceuticalethics.com

  • Jan 2008 - Jun 2013

  Provision of compliance training and support to pharma companies in UK and Europe working alongside Dr Sian Walker



Celgene

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Medical and Regulatory Affairs Director

  • Jun 2006 - Dec 2007

  Celgene UK and IrelandI joined Celgene Ltd, a US based pharmaceutical Company, in order to recruit and build a complete medical department for the UK subsidiary prior to the launch of a novel treatment for haematological malignancy. I recruited a team of 10 and led the establishment of the regulatory, drug safety, medical information and clinical research processes good governance demands.In addition, given the particular nature of the product concerned, I led the development and implementation of a complete safety risk minimisation plan agreed in meetings with both the UK and Ireland regulatory authorities. Agreement to the plan was a pre-requisite of product launch which has now been successfully achieved.



AstraZeneca

• United Kingdom
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Director European Regulatory Affairs

  • May 2004 - May 2006

  In this role I matrix managed the heads of regulatory affairs for 10 European markets across all AZ therapy areas ensuring consistent implementation of regulatory and market access strategy. I was responsible for the development of European regulatory strategy for one compound in the CV/metabolic therapy area.Within my time in this role over a period of 6 months I had accountability for the complete restructure of the medical and clinical research departments of a European subsidiary and the recruitment of a new medical director.

• Head of Medical Affairs

  • Apr 2002 - Apr 2004

• Medical Affairs Manager

  • Jul 2000 - Mar 2002



MSD UK

• Medical Advisor

  • Jun 1998 - Jun 2000

  I provided medical advice and drug safety support in both the cardiovascular and respiratory therapy area.



Sanofi Winthrop UK

• Clinical Research Manager

  • Oct 1996 - May 1998

  I managed a team of 4 clinical research associates in the delivery of phase II to IV studies in osteoporosis, cardiovascular disease and rheumatology. I gained hands-on experience in clinical trial protocol development and delivery.



NHS

• Hospitals and Health Care
• 700 & Above Employee

• GP

  • Oct 1993 - Sep 1996