CV of AFFILIATE MEDICAL DIRECTOR / MEDICAL DIRECTOR , looking for a job of MEDICAL AFFAIRS IN PHARMACEUTICS OR IN BIOTECH / therapies.enligne-ch.com

Cv de MEDICAL DIRECTOR

French Licensed M.D., MSc, Master in Pharmacology, Experienced in Medical Affairs for Pharmaceutics in France and in the US, in multiple therapeutic areas including Oncology, Hematology, Inflammatory Diseases, Neurology, Cardiovascular Diseases. Also experienced in Global R&D External Innovation.

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CV Code: 58d8f99b0a775997
Date of last connection: 2017-03-27

Mr. Fr... G...

....

92330 SCEAUX
France

Current situation:

Current industry: ABBVIE

Size of the company: More than 1,000 employees

Current position: AFFILIATE MEDICAL DIRECTOR

Number of years spent at this position: 3-5 years

Number of persons you managed: 51-100 persons

Annual salary: 200000.00 EUR

Total working experience: more than 15 years

Availability: Immediate availability

Job sought:

Positions: MEDICAL DIRECTOR, GLOBAL THERAPEUTIC AREA LEAD, EXPATRIATE MEDICAL AFFAIR LEAD

Industry: PHARMACEUTICS, BIOTECH, INTERNATIONAL ACADEMIC / HEALTH ORGANISATIONS

Desired type of contract: open-ended contract

Desired working time: Full-time

Minimum annual salary desired: 180000.00 / 0.00 EUR

Education:

Highest educational level completed: number of years studied and completed with a diploma after highschool : +11

Last diploma : MEDICAL DOCTOR

Current educational level : +11

Other training courses :


Divers :

Geographical mobility: Country : Belgium, France, Germany, Switzerland, United Kingdom, United States

Known Tools / Software/ Methods MEDICAL EXPERTISE FOR GLOBAL AND GENERAL MANAGEMENT (CEO), STRATEGIC PLANS, MARKETING PLANS AND REGULATORY REVIEW, GENERAL MANAGEMENT IN MEDICAL AFFAIRS INCLUDING THERAPEUTIC AREAS CLINICAL OPERATIONS MEDICAL INFORMATION QUALITY CONTROL PHARMACOVIGILANCE, , KEY EXPERT PARTNERSHIPS AND RELATIONSHIP, MEDICAL COMMUNICATION INCLUDING PRESS CONFERENCE AND INTERVIEWS, SUPPORTING FILINGS AND RELATIONSHIPS WITH HEALTH AUTHORITIES


HGV, LGV, special vehicles licences MEDICAL DOCTOR, MASTER IN SCIENCE, CLINICAL AND EXPERIMENTAL PHARMACOLOGY, CARDIOVASCULAR DISEASES, INTERNAL MEDICINE, INTENSIVE CARE AND MEDICAL REANIMATION; EXPERIENCE IN CONDUCTING MEDICAL AFFAIRS IN ONCOLOGY HEMATOLOGY RHUMATOLOGY DERMATOLOGY GASTROENTEROLOGY HEPATOLOGY (HEP C) NEUROLOGY NEONATALOGY PSYCHIATRY CARDIOVASCULAR CARDIOTHROMBOTIC CARDIOMETABOLIC UROLOGY ; EXPERIENCE IN GLOBAL R&D EXTERNAL INNOVATION


Languages English : Working language


Resume:

Mr. Fr... G...

....

92330 SCEAUX
France

Date of birth: August 13,
1961

Citizenship: French



CURRICULUM VITAE

(as of March 2017)





























French Licensed
M.D., Master in Clinical and Experimental Pharmacology, Experienced in Conducting
of Medical Affairs in Pharmaceutics (in France and in the US), notably in
Oncology, Hematology, Virology (Chronic C. Hepatitis), Rheumatology,
Dermatology, Gastro-Enterology, Internal Medecine and Inflammatory Diseases,
Neurology, Psychiatry, Urology, Cardiovascular Prevention and Diseases,
Cardiometabolic Diseases, and Thrombosis. Also experienced in Global R&D External
Innovation.




Professional
Cursus in Pharmaceutics:



2014-17 AbbVie France Medical Director, Global Medical
Affairs:


Head of Abbvie France Affiliate Medical Direction (n=75), within AbbVie Global
Medical Affairs.

In charge of Clinical Operations, Medical Information, Pharmacovigilance
and Quality Control, Medical Expertise and overall Management of the Conducting
of the Abbvie French Affiliate Medical Affairs (including Medical Liaison
Teams) for its Portfolio Therapeutic Areas (Rheumatology, Dermatology,
Gastro-Enterology, Internal Medecine, Virology HIV and Chronic C., Hemato-Oncology, Neurosciences
and Neonatology. Notably:

·
Pre-Authorization Access Programs, in coordination
with the French Health Authorities

·
Medical Expertise for Market Access Filings and
Medical Hearings by HTA Body for Reimbursements

·
Management of the Relationship with French Health
Authorities for Medical Expertise in Regulatory Exchanges

·
Drug Safety Monitoring and Risk Management Plan Monitoring

·
Observational Studies, including HTA Body-required
Studies, Epidemiology and RWE Studies, Support and Follow-up of
Investigator-Sponsored Studies, and data Publication

·
R&D Clinical Trials submission to the French Health
Authorities and coordination with local R&D Site Management Unit

·
Management of the Relationship and the Collaboration
with Key External Experts and of the Partnerships with Key Scientific
Associations,

·
Medical Review and Approval of Patient Support Programs
(PSP) and Governance of the PSP Internal Advisory Board

·
Medical Review and Approval of External Communication,
including Medical Expertise for Regulatory Approbations

·
Medical and Scientific Communication : Press
Conference, Radio and Newspaper Interviews, Scientific program of Symposia,
Advisory Boards, and Scientific Meetings with Key External Experts

·
Medical Expertise and Advising for the Affiliate
Management Team and for the General Manager (CEO), as Member of the Affiliate
Management Team, for Abbvie France Affiliate Communication and Activities in
its whole Portfolio Therapeutic Areas, including R&D Portfolio, notably Medical Resourcing
and Budget, 1-Yr and Long Range Brand Plans.



2010-14: sanofi-aventis Global R&D External Innovation
& Science Policy:


Scientific Collaborations with Academia and Biotech
Companies for Innovative Partnerships and Licensing-in for the sanofi-aventis
Global R&D Portfolio:

Contracting (Worldwide): Agreement Negotiation
and Finalization with R&D, Legal, IP, Purchase and Finance
Alliance Management (Europe) for R&D Strategic
Alliances
Support to In-Silico Scouting, Eastern
Asia–Pacific scouting, participation to setting up of the IT Systems for External
Innovation


2007-10: Senior Medical Director, Thrombosis
franchise, Medical Affairs, sanofi-aventis Inc., USA:


Head of US Throbosis Medical Team: Transversal Management in Matrix Organization
with Clinical Trial Operations, Biostatistics, Data Management, Publications,
HEOR, Medical Liaisons, Medical Education, Pharmacovigilance, notably:

·
Design, Deployment and Follow-up of the Thrombosis 1-Yr
Medical Plans, in line with Lovenox® Brand Strategy; Organization and Leading
of the Enoxaparin US Core Medical Team ; Medical Guidance to the Lovenox® US Brand
Team

·
Management of the relationship and partnership with
top Key US External Experts and Scientific Associations in Cardiovascular Thrombotic
diseases; Management of Advisory Boards and Scientific Meetings in these
therapeutic domains

·
Data-Driven (Observational Studies, Clinical Trials,
Investigator-Sponsored Studies, Health Outcomes/Economics studies) Scientific Support
to Cardiovascular Thrombosis Team Strategic and Operational Plans, Evidence-based Medicine Publication

·
Drug Safety Monitoring

·
Evidence-based Medicine Data Dissemination by Medical
Liaisons (n=10)

·
Medical Review and Approval of the Lovenox® Brand
Material for Regulatory Compliance

·
US Medical Affairs Coordination Thrombosis R&D Project Teams


2004-07: Senior Medical Director, Cardiometabolic Business
Unit (BU), sanofi-aventis France:


Head of Medical Affairs for the sanofi-aventis France Portfolio in the Cardiovascular
and Diabetes Therapeutic Area (n=15): Overall
Management of the Medical Operations, including including Set-up then Management of the Medical Liaison Team, Clinical Trials and Observational studies and Clinical Plan, Management of the Relationship and Collaboration with Key External Experts, Management of National and International Expert Advisory Boards, Management of Partnerships with Scientific Associations, Medical and Scientific Expertise for External Communication, and for Medico-Marketing or Strategic Plans, Medical and Scientific Expertise for External Communication
and Regulatory Approbation of Promotional Material, and for Medico-Marketing or
Strategic Plans.


2003-04: Deputy to VP. Medical Affairs, Internal Medicine
Business Unit (BU), sanofi-synthelabo France:


Medical Advisor dedicated to the sanofi-synthelabo France Portfolio in Thrombosis/Internal
Medicine Therapeutic Area (transversal management) Medical / Scientific Expertise
and Advising for the Regulatory Compliance of External Communication, Medical Scientific Expertise for Medico-Marketing and Strategic Plans, Market Access Filing and submission to HTA Body in France.



2001-03: Associate VP. Medical Affairs,
sanofi-synthelabo France:


Deputy to the sanofi-synthelabo French Affiliate V.P. Medical Affairs,
notably in charge of:

·
Medical/Scientific Expertise and Advising for the
Medical Operations and the External Communication sanofi-synthelabo French
Affiliate regarding its whole Portfolio (notably Cardiovascular, Thrombosis,
Oncology, Internal Medicine, Neurology/Psychiatry), including R&D Portfolio

·
Medical /Scientific Expertise and Advising for the Regulatory
Compliance

·
Support of Medical Organizations and Activities in the
Affiliate Business Units

·
Management of Sanofi-synthelabo France Medical
Operations (n= 110): R&D Clinical Trials Dpt. (CRU), Pharmacovigilance
Dpt., and Medical Information Dpt.



1996-2001: Cardiovascular BU Medical Director, Sanofi France

Head of Medical Affairs for sanofi-synthelabo France Portfolio in Cardiovascular
Therapeutic Area (n=20): overall Management
of Medical Operations, including Medical Liaisons Team,
Clinical Trials Observational studies and Clinical Plan, Management of the
Relationship and Collaboration with Key External Experts and of the Partnerships
with Scientific Associations, Medical and Scientific Expertise for External Communication
and Regulatory Approbation of Promotional Material, and for Medico-Marketing or
Strategic Plans.



1994-96: Nadroparin (Fraxiparine) Medical Manager, Sanofi-Winthrop
France


Phase IIIb and IV trials, Management of the relationship with Key
External Experts, Medical sourcing, Scientific Communication in Public Meetings.





Professional Cursus outside Pharmaceutics:
·
1992-94: Fellowship in Internal Medicine and Intensive Care (C.C.A Réanimation
Médicale), CHU Garches, Paris-Sud University, France
·
1988-90: Head of French Embassy Medical Dpt., Moscow USSR, French Foreign Office
·
1986-88, 1990-92: Resident in Cardiology, Internal Medicine, Oncology, Pharmacology,
Paris, France


Background and
Training:


·
M.D . Graduate, UFR X. Bichat, Paris VII University,
France, 1992

·
Licensed in Cardiology and Cardiovascular Diseases
(DES), UFR X. Bichat, Paris VII University, France, 1992

·
Master in Clinical and Experimental Pharmacology
(DEA), P. et M. Curie University Paris, France, 1992

·
Licensed in Internal Medecine and Medical Intensive
Care (DESC), Paris-Sud University, France, 1994

·
Coach for General Management (CS Consulting) 1998

·
Training Courses in Strategic Marketing (StratX,
Compass) 1998

·
Training Courses in General Management (Manager of
Managers) 1997-99

Cover letter

Mr. Fr... G...

....

92330 SCEAUX
France

French Licensed M.D., MSc, Master in Pharmacology, Experienced in Medical Affairs for Pharmaceutics in France and in the US, in multiple therapeutic areas including Oncology, Hematology, Inflammatory Diseases, Neurology, Cardiovascular Diseases. Also experienced in Global R&D External Innovation.

Dear
Sir, Madam,



As you will see in my attached résumé, I conducted Medical Affairs in several
types of organizations, in Large Business Units or Affiliates, and within
Global Organizations. I am also experienced in American Ways of Working,
notably thanks to a 4-Yr long professional experience on the US soil, as an
expatriate, and a 4-Yr long experience in external innovation for Global
R&D (Scouting, Contracting Alliance Management).



I can run Medical Affairs in Pharmaceutics Organizations of any size in France
or in English-speaking countries, both at Affiliate, Area or Global level, in
any therapeutic area. I am also open to conducting Medical activities in other
domains than drug–related therapeutic areas, such as in technology (such as
equipment for Apheresis, or Blood Donation ), isotope-based therapies or even
Specific Public Health Policies.



My wish is to support organizations dedicated to addressing heavy medical needs
through drug-or not-drug based approaches, notably innovative ones, with
providing my knowledge and know-how, or through expanding my personal
experience in domains which could be new to me.



I think that my clinical, my scientific background and my professional
experience in Medical Affairs, notably (but not only) in clinical operations,
medical information, safety monitoring, medical communication, management of
partnerships with Key Experts, management of relationship with health
Authorities, connected support of R&D, can meet expectations in terms of
recruitment needs for Pharmaceutical Firms, Biotech Companies or International
Public Health Organizations, in this area of expertise and activities.



To summarize, I think that joining my experience and my energy to the
objectives of such types of organizations will be very exciting to me and may
be of particular interest for these organizations.



I hope this letter will find you well.



Best regards,

Mr. Fr... G



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