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BoosConsulting was founded by Monika Boos, MD, PhD, LL.M. and pharmaceutical-technical assistant with long-time professional experience in pharmacy, hospital, medical practice and the pharmaceutical industry.

 

Dr. Boos benefits from 14 years of pharmacovigilance experience that was built on ten years of permanent employments in international pharmaceutical companies comprising extensive hands-on experience, as well as more than five years of operations in leadership positions (national & international teams, matrix structures, forums including worldwide PV responsibility for established products and development compounds), lastly as German Graduated Plan Commissioner, Deputy EU QPPV and Head of Corporate Pharmacovigilance.

 

                                                                                                      

While searching for an opportunity to combine both my pharmaceutical as well as my medical qualifications, I joined the pharmaceutical industry with a focus on drug safety. Even after more than14 years my passion for this field of expertise is still undiminished and I am pleased to contribute my expertise (that is additionally supported by a Master of Laws degree in the special area of pharmaceutical law) to further ensure patient’s safety.

                                                                                                                     

 

Brief CV of Dr. Monika Boos, LL.M.:

1991-1996:

Apprenticeship for pharmaceutical-technical assistant followed by pharmacy employment

1996-2004:

Studies of human medicines (MD), followed by a PhD thesis at the Institute for Clinical Pharmacology at the Johann-Wolfgang-Goethe University Frankfurt with subsequent employments as physician in the area of cardiology and gastroenterology at hospital and medical practice

2004-2014:

For around 10 years different pharmacovigilance positions with increasing responsibilities in international pharmaceutical companies with headquarters in Germany, Japan and Sweden:

   

2004-2007: Medical Advisor Drug Safety, Regional Centre Europe, Boehringer Ingelheim

   

2007-2011: Global Drug Safety, Merck KGaA

              2010-2011: Medical Director, Head Medical Safety Evaluation Group Fertility / Metabolic Endocrinology
          2008-2010: Group Leader Endocrinology, Medical Safety Group General Medicine
          2007-2008: Drug Safety Officer, Medical Safety Group General Medicine
   

2011-2013: Senior Pharmacovigilance Manager, Deputy EUQPPV, Head of Post Marketing Safety PV Europe,   Deputy Head PV Region Europe (Post Marketing Safety & Clinical Safety), Chair of the Global Safety Scientist    Team, Otsuka Frankfurt Research Institute

   

2013-2014: Head of Corporate Pharmacovigilance, Deputy EUQPPV and German Graduated Plan Officer, MEDA Pharma GmbH & Co. KG

2014:

Foundation of BoosConsulting for independent, tailored and flexible consultancies and services with medical-pharmaceutical scope

2015-2017:

Pharmaceutical laws study program, Philipps University Marburg (Faculty of Law), Master of Laws degree (LL.M.)

 

Further activities:

Elected Chair of the division „Pharmacovigilance“ of the German Association of Pharmaceutical Medicine (DGPharMed e.V.)

Member of the International Federation of Associations of Pharmaceutical Physicians and Pharmaceutical Medicine (IFAPP)

Member of the Drug Information Association, Inc. (DIA)

Individual member of the “Research Center for Pharmaceutical Law” sponsoring society at the Philipps University Marburg (Germany)

Review Board member for the journal "PM QM" (specialised magazine for pharmaceutical medicine and quality management)

Lecturer at the Carl Remigius Medical School (medical faculty of the university Hochschule Fresenius)

Board Memeber of the German Association of Pharmaceutical Medicine (DGPharMed e.V.)

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