Brigitte LampoKattestraat, 282811 HombeekTel: +32 15 34 74 00Mobile: + 32 475 71 77 84

I. Personal Data

Place and date of birth: Gent, 23 March 1965Marital Status: Married, 2 childrenNationality: Belgian

II. Career (in chronological order, most recent function first)

Temporary assignment as Functional Head of the Country Clinical Site Operations – United States of America

Senior Manager Development Operations – Belgium, Luxemburg, Netherlands and Israel - Amgen N.V (from March 2014)Management of the Clinical Site management Team (around 100 people) and all phase interventional/ observational studies (on average over 70 active studies) in Belgium, Luxemburg, The Netherlands and Israel. Leading the integration of study responsibilities from the Netherlands into the Belgian Hub. Member of multiple workgroups focused on global change initiatives.

Senior Manager Development Operations – Belgium, Luxemburg, Israel and Turkey - Amgen N.V (from Jan 2013)Management of the Global Clinical Site management Team (over 75 people) and all phase interventional/ observational studies (on average over 70 active studies) in Belgium, Luxemburg, Israel and Turkey. Leading the transition of study responsibilities from Belgian Hub to South Africa and Turkey, newly created stand-alone countries for clinical operations.

Senior Manager Development Operations – Belgium, Luxemburg, Middle East, Africa and Turkey - Amgen N.V (from Sep 2008)Management of the Global Clinical Site management Team (over 50 people) and all phase interventional/ observational studies (on average over 70 active studies) in Belgium, Luxemburg, Israel, South Africa, Turkey and Malta.

Senior Manager Clinical Field Operations – BELUX - Amgen N.V (from Jan 2006)Management of the Clinical Development Team and clinical and medical affairs interventional/ observational studies in Belgium and Luxemburg. Development Operations Manager – BELUX - Amgen N.V (from August 2002)Management of the Clinical Development Team and clinical and medical affairs clinical studies in Belgium and Luxemburg.

European Clinical Working Group Leader/ Oncology Bristol Myers Squibb – Pharmaceutical Research Institute (From January 2002)Management of several phase 2 and 3 oncology projects

European Clinical Working Group Leader/ NeuroscienceBristol Myers Squibb – Pharmaceutical Research Institute (From August 1999)Management of the European part (4 European/ Intercontinental protocols) of a worldwide development program with an antipsychotic agent in different indications ( Acute Schizophrenia (22 countries), Acute Mania ( 15 countries),

Recurrence prevention in Bipolar Disorder ( 14 countries), Psychosis in dementia (10 countries).

Project Manager – Oncology TherapeuticsQuintiles (merged with BRI end 1996, till July 1999)Project management of multiple projects in oncology.The project management role involves integration management, scope management, time management, cost management, quality management, resource management, communication management and risk management throughout the lifespan of the projects.

Furthermore involved in client meetings, proposal discussions, staff recruitment, management of smaller trials, development of financial tracking systems and project databases.

International Project Manager/ Group Manager Clinical OperationsBRI International (merged with Health Care Research, 1994- 1996)Coordination of the planning and implementation of a worldwide study (oncology) in Europe, South Africa and India (170 centers, 37 countries).Direct responsibility for Western and Eastern Europe, Africa, Middle East and India (85 sites, 21 countries).Involved: Responsibility for project maintenance and oversight: project timelines and resourcing planning, proposal discussions, protocol development, client contacts, budget management, quality management, set up and coordination of central radiographic imaging collection and review, investigator meeting organization, overall oversight of third parties (central lab, drug distribution)Line management responsibility for 8 internal people.

International Monitoring Coordinator Health Care Research, Mechelen (1992 – 1995)Coordination of the planning and implementation of a multi - centre study (CNS) in Europe, (70 centers, 900 patients).This role consisted of being the primary contact with sponsor of trial, protocol and CRF review, coordination of 8 CRA’s, investigator meeting organization and presentation, responsibility for study logistics, budget, quality and timelines.

Clinical Research AssociateHealth Care Research (1991-1993)Site selection and monitoring of Ph 2 and Ph 3 clinical studies in rheumatology, neurology and oncology.Monitoring of sites in Belgium, the Netherlands, Germany, France, Greece and Portugal.

Scientific collaborator (1989- 1991)- Ghent University – Faculty of Medicine – Lab for Movement

Analysis (50%)- Ghent University – Higher Inst. for Physical Education, Lab for

Movement Sciences (50%)

III. Education

Higher education – Ghent University – Belgium

- Master of Science in Rehabilitation Sciences and Physiotherapy, 1988, Ghent University - Magna Cum Laude

- Master of Science in Physical Education and Movement Sciences, 1986, Ghent University - Magna Cum Laude

- Academic Teaching certificate in Physical Education and Movement Sciences, Faculty of Psychology and Educational Sciences, 1986, Ghent University, Cum Laude

IV. Languages

Dutch: mother tongue French: written and spoken, goodEnglish: written and spoken, good German: written and spoken, fair