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Karen MD

Medical Team Leader Cardiovascular

Transforming Science into Value as Head of Medical Affairs Belgium & Luxembourg at Boehringer Ingelheim

Brussels Area, Belgium

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Karen MD's Email Addresses & Phone Numbers

Karen MD's Work Experience

Boehringer Ingelheim

Medical Team Leader Cardiovascular

March 2015 to Present

Amsterdam Area, Netherlands

Boehringer Ingelheim

Medical Affairs Operations Southern France

March 2013 to February 2015


Medical Advisor France

May 2010 to March 2013

Karen MD's Education

Université Paris Descartes (Paris V)

University Diploma Pharmacoeconomics

2011 to 2012

Ecole de Management de Marseille

Master in Healthcare Company Management Healthcare Management

Université de la Méditerranée (Aix-Marseille II)

DIU CESAM (University Diploma) Statistics applied to clinical trials

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Karen MD's Estimated Salary Range

About Karen MD's Current Company

Boehringer Ingelheim

Medical Team Leader Cardiovascular European Regional OPU MIDI (cardio/thrombosis) Pradaxa (dabigatran), Praxbind (idarucizumab)

Frequently Asked Questions about Karen MD

What company does Karen MD work for?

Karen MD works for Boehringer Ingelheim

What is Karen MD's role at Boehringer Ingelheim?

Karen MD is Medical Team Leader Cardiovascular

What is Karen MD's personal email address?

Karen MD's personal email addresses are k****[email protected], and k****[email protected]

What is Karen MD's business email address?

Karen MD's business email addresses are not available

What is Karen MD's Phone Number?

Karen MD's phone (**) *** *** 435

What industry does Karen MD work in?

Karen MD works in the Pharmaceuticals industry.

About Karen MD

📖 Summary

From robust scientific data to evidence-based everyday healthcare practice //please use only e-mail or linkedin messaging to contact me// Medical Project Leadership for Health Care Industries with experience in : Clinical Medicine Drug Development Project Management Orphan Drugs Interactions with Stakeholders Medical Communication Medical Information Specialties: Clinical Medicine; DIU CESAM (medical statistics); DIU FIEC (clinical trials); Healthcare Management; Medical Devices; Animal ExperimentsMedical Team Leader Cardiovascular @ Medical Team Leader Cardiovascular European Regional OPU MIDI (cardio/thrombosis) Pradaxa (dabigatran), Praxbind (idarucizumab) From March 2015 to Present (10 months) Amsterdam Area, NetherlandsMedical Affairs Operations Southern France @ Regional Medical Affairs in Internal Medicine: Cardiology, Thrombosis, Respiratory (COPD, asthma, Idiopathic Pulmonary Fibrosis) for Southern France Special involvement in dabigatran antidote (idarucizumab) project and Idiopathic Pulmonary Fibrosis team From March 2013 to February 2015 (2 years) Medical Advisor France @ Medical Projects (both field & HQ based) in Immunotherapy and Intensive Care & Emergency Medicine (thrombosis) 2 International Business Team core member Medico-Marketing activities, KOL development, observational studies, Investigator Initiated Studies, Medical education, training for sales, field Medical Liaison activity, trial protocol proposal, CRO management Medical Information, external query management From May 2010 to March 2013 (2 years 11 months) Medical Advisor MabThera RA @ Medical Project Management in Immuno-Rheumatology (MabThera/Rituximab, monoclonal antibody used in Rheumatology, Autoimmune Diseases and Onco-Haematology) Medico-Marketing activities, Clinical Studies From 2010 to 2010 (less than a year) Director of Projects & Operations @ - General management, multi-disciplinary project management - Public relations with Stakeholders (including patients’ associations, healthcare professionals, academia, university hospitals, research organisms, bioclusters, associations etc), - Representation of the company in all events with key Stakeholders (congresses, boards, public events) - Communication management - Management of an orphan medicinal product designation request from EMEA (medical writing of the application, managing application process with EMEA COMP, results - orphan designation No EU/3/08/531 successfully obtained in 2008), and FDA (obtained in 2009) - Management of the follow-up process for orphan designations - Management of a scientific advice request from AFSSAPS, EMEA - Day-to-day management of the team, commercial negotiations From December 2006 to November 2009 (3 years) Medical Information Officer @ EU trainee programme - created and managed a database and tracing tool of stakeholders, participated in interactions with key interested parties (including patients and consumers organizations, healthcare professionals organisations, learned societies etc) - managed external queries from patients and healthcare professionals - participated in meetings of several Scientific Committees and Working Parties, including the Committee of Human Medicinal Products (CHMP), PDCO, COMP, CAT, CVMP, HMPC, as well as Working Parties (Efficacy, Safety, Pharmacovigilance etc) - acquired an extensive knowledge of European pharmaceutical legislation, Community procedures, rules and mechanisms of EMEA’s internal functioning From September 2008 to March 2009 (7 months) London, United KingdomResident Physician @ - medical information provision to general public and healthcare professionals (mainly to physicians, including hospital emergency services, pharmacists and occupational and public health specialists) about intoxication by natural toxins, drugs, chemical products, cosmetics etc - medical information provision about drug adverse effects - reception and initial treatment of ICSR (mainly from general public), liaising pharmacovigilance team, management of safety alerts for drugs and food - work with toxicology and adverse effects database (input, output, statistics), bibliographic research From May 2006 to May 2007 (1 year 1 month) Resident Physician @ resident physician in various otolaryngology and head & neck surgery departments (including pediatrics, head & neck oncology, audiophonology, cochlear implants) - participation in clinical medical, surgical and outpatient activity - organisation of clinical staff meetings, grand rounds - scientific writing activity (research papers, books chapters) - training and courses for medical students - organisation of and participation in scientific events, workshops and congresses in collaboration with stakeholders - management of information & communication projects via internet and multimedia supports From 2001 to 2005 (4 years) Marseille Area, FranceUniversity Diploma, Pharmacoeconomics @ Université Paris Descartes (Paris V) From 2011 to 2012 Master in Healthcare Company Management, Healthcare Management @ Ecole de Management de MarseilleDIU CESAM (University Diploma), Statistics applied to clinical trials @ Université de la Méditerranée (Aix-Marseille II)DIU FIEC (University Diploma), Training for a Clinical Trial Investigator @ Université de la Méditerranée (Aix-Marseille II)University Diploma, Immunology & Biotherapies @ Université Pierre et Marie Curie (Paris VI)University Diploma, Medical Devices and Biologicals @ Université Denis Diderot (Paris VII)University Diploma on Animal Experiments, Animal Experiments @ Université de la Méditerranée (Aix-Marseille II)Postgraduate training, Postgraduate medical training in Public Health @ Université de la Méditerranée (Aix-Marseille II)Postgraduate training, Postgraduate medical training in Otolaryngology and Head & Neck Surgery @ Université de la Méditerranée (Aix-Marseille II)University Diploma, Multimedia and Pedagogy in Healthcare @ Université du Droit et de la Santé (Lille II)M.D., human medicine @ YSMU Medical School Karen MD is skilled in: Clinical Research, Pharmacoepidemiology, Medical Education, Scientific Communications, Drug Development, Biostatistics, Pharmacovigilance, Medical Devices, Clinical Trials, Clinical Development, Pharmaceutical Industry, Rheumatology, Clinical Pharmacology, FDA, Oncology

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In a nutshell

Karen MD's Personality Type

Extraversion (E), Sensing (S), Feeling (F), Judging (J)

Average Tenure

1 year(s), 11 month(s)

Karen MD's Willingness to Change Jobs



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