Sarah Cox
Pharmacovigilance Consultant & EEA/UK QPPV at Cox PharmaConsulting- Claim this Profile
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Bio
Marco Taglietti
When Sarah worked for me, I assigned her to a large, complex project that she managed successfully and on time. It was an outstanding performance. She is a driven employee who get things done and she pursues the goals of the projects assigned to her with relentless energy, great enthusiasm and superb efficiency.
Jon Eversham
I worked with Sarah on a project to deploy an IT system supporting the tracking of Pharmacovigilance (PV) adverse events, across three geographic regions (Europe, North America, Latin America). Sarah acted as the PV Business Lead and Subject Matter Expert, whilst I was project managing the system configuration and deployment. In my dealings with Sarah, I found her to demonstrate great enthusiasm and PV expertise, succinctly defining the requirements of the business and ensuring that the correct solution would be released to the user community. Sarah showed great flexibility and thoroughness, particularly in testing, to ensure that the system worked as expected, and to complete testing within hard deadlines.
Marco Taglietti
When Sarah worked for me, I assigned her to a large, complex project that she managed successfully and on time. It was an outstanding performance. She is a driven employee who get things done and she pursues the goals of the projects assigned to her with relentless energy, great enthusiasm and superb efficiency.
Jon Eversham
I worked with Sarah on a project to deploy an IT system supporting the tracking of Pharmacovigilance (PV) adverse events, across three geographic regions (Europe, North America, Latin America). Sarah acted as the PV Business Lead and Subject Matter Expert, whilst I was project managing the system configuration and deployment. In my dealings with Sarah, I found her to demonstrate great enthusiasm and PV expertise, succinctly defining the requirements of the business and ensuring that the correct solution would be released to the user community. Sarah showed great flexibility and thoroughness, particularly in testing, to ensure that the system worked as expected, and to complete testing within hard deadlines.
Marco Taglietti
When Sarah worked for me, I assigned her to a large, complex project that she managed successfully and on time. It was an outstanding performance. She is a driven employee who get things done and she pursues the goals of the projects assigned to her with relentless energy, great enthusiasm and superb efficiency.
Jon Eversham
I worked with Sarah on a project to deploy an IT system supporting the tracking of Pharmacovigilance (PV) adverse events, across three geographic regions (Europe, North America, Latin America). Sarah acted as the PV Business Lead and Subject Matter Expert, whilst I was project managing the system configuration and deployment. In my dealings with Sarah, I found her to demonstrate great enthusiasm and PV expertise, succinctly defining the requirements of the business and ensuring that the correct solution would be released to the user community. Sarah showed great flexibility and thoroughness, particularly in testing, to ensure that the system worked as expected, and to complete testing within hard deadlines.
Marco Taglietti
When Sarah worked for me, I assigned her to a large, complex project that she managed successfully and on time. It was an outstanding performance. She is a driven employee who get things done and she pursues the goals of the projects assigned to her with relentless energy, great enthusiasm and superb efficiency.
Jon Eversham
I worked with Sarah on a project to deploy an IT system supporting the tracking of Pharmacovigilance (PV) adverse events, across three geographic regions (Europe, North America, Latin America). Sarah acted as the PV Business Lead and Subject Matter Expert, whilst I was project managing the system configuration and deployment. In my dealings with Sarah, I found her to demonstrate great enthusiasm and PV expertise, succinctly defining the requirements of the business and ensuring that the correct solution would be released to the user community. Sarah showed great flexibility and thoroughness, particularly in testing, to ensure that the system worked as expected, and to complete testing within hard deadlines.
Experience
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Cox PharmaConsulting
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United Kingdom
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Pharmacovigilance Consultant & EEA/UK QPPV
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2010 - Present
Pharmacovigilance Consultancy, EEA/UK QPPV Contracts & Inspection Management. CAPA & Implementation of new PV systems. Selection/transition to a new PV Service Provider. Pharmacovigilance Consultancy, EEA/UK QPPV Contracts & Inspection Management. CAPA & Implementation of new PV systems. Selection/transition to a new PV Service Provider.
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Stiefel, a GSK company
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United States
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Pharmaceutical Manufacturing
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300 - 400 Employee
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Director Global Pharmacovigilance Operations
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Nov 2007 - Apr 2010
With a global scope, maintain regulatory compliance. Support the continued global development of pharmacovigilance.
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Global Project Leader (Pharmacovigilance Global Implementation) & Deputy QPPV
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Mar 2005 - Nov 2007
The creation and leadership of the global Pharmacovigilance Implementation Team. The team created a new global function; recruiting a new team, implementing the new structure & responsibilities, a safety database, all global procedures, training and Safety Data Exchange Agreements. Responsibilities extend to all of Stiefel’s dermatology products which include Pharmaceuticals (Drugs, some Devices) and Cosmeceuticals.Line Management and/or matrix management of the Global Pharmacovigilance Group in the UK, USA and Brazil. Deputy QPPV.
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Deputy QPPV & Senior Clinical Research Associate
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May 1999 - Feb 2005
Responsibilities (Clinical Research) include Line Management, Deputising Head of Clinical Research, Clinical Project Management (Phases I-IV), Contract Management (CRO’s, Freelancer’s), Clinical Study Design, Medical Writing (Study Reports & other, as required). Responsibilities (Pharmacovigilance) also extended to a second role as deputy QP for Pharmacovigilance (post-marketing) and to managing the multiple contractors that constituted the Pharmacovigilance function. Authoring PSUR and other safety reports.
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Clinical Research Associate
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Jan 1997 - Jan 1998
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Clinical Research Associate
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Nov 1993 - Dec 1997
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Clinical Research Associate
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Jul 1993 - Oct 1993
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Clinical Research Associate (student placement)
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Aug 1989 - Sep 1990
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Education
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1987 - 1991
King's College London
BSc Hons, Biotechnology
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