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Philippe Ronga Md-Independent Medical Affairs & Clinical Development Consultant

Philippe Ronga Md - Independent Medical Affairs & Clinical Development Consultant - profile avatar
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Available
Bad Homburg, Germany

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Experience

Jan 2025 - Present
Frankfurt am Main, Germany

Founder | Senior Clinical & AI Strategy Advisor to PE/VC & Boards

Nexevan Advisory

Position summary
Founder | Senior Clinical & AI Strategy Advisor to PE/VC & Boards at Nexevan Advisory
Industries
Biotechnology
Healthcare
Pharmaceutical
Business areas
Information Technology
Strategy

Nexevan Advisory provides independent senior clinical and AI strategy support to PE/VC funds, Boards, and Leadership teams investing in or scaling clinically complex Healthcare businesses.

I support clients across pre-investment diligence, portfolio value creation, evidence and adoption strategy, cross-border growth, AI Governance, strategic-buyer readiness, and Board advisory.

The advisory scope spans BioPharma, MedTech, HealthTech, Diagnostics, and specialty Healthcare services, supported by deep expertise in Oncology, Haematology, Rare Diseases, and Internal Medicine.

Engagements include 7-14-day red-flag reviews, 2-6-week strategic deep dives, project-based mandates, Board and strategic advisory retainers, and fractional executive support.

Sep 2021 - Dec 2024
Frankfurt am Main, Germany

Global Medical Lead - Knowledge Management Capabilities Development - GMA Oncology

Merck KGaA

Position summary
Global Medical Lead - Knowledge Management Capabilities Development - GMA Oncology at Merck KGaA
Industries
Healthcare
Pharmaceutical
Business areas
Operations
Project Management
Research and Development
Strategy

→ GLOBAL MEDICAL AFFAIRS ONCOLOGY DIRECTOR; MEDICAL EXCELLENCE, MULTI-COUNTRY & STRATEGIC OVERSIGHT

  • Led strategic planning for Global Medical Affairs, ensuring cross-functional collaboration and defining clear strategy; chaired Medical Decision Board.
  • Ensured Medical Affairs strategic alignment with Corporate and Commercial goals, providing insights across global markets.
  • Structured program, IST (Phase I & II), Clinical Research, and Regulatory Affairs strategies key to reaching Medical Affairs goals for metastatic colorectal cancer (mCRC).
  • Coordinated matrix, multi-country team efforts (up to 60 countries) for meaningful insights.
  • Led Evidence Generation, Market Access / HEOR, and Medical Education, leveraging skills in GI malignancies, targeted therapies, and Liquid Biopsy skills.
  • Administered training and materials development for MSLs.

→ DIGITAL ENGAGEMENT & DATA GENERATION ACHIEVEMENTS:

  • Attracted thousands of attendees (physicians) with live webinar series featuring top experts, with content customized to EMEA, APAC (including China and Japan), and LATAM regions. Facilitated discussion using surveys and asynchronous / chat forums for Advisory Boards in multiple therapeutic areas with 100+ experts.
  • Leveraged new platforms to elicit Head & Neck, Gastrointestinal, and Lung oncology therapeutic specialist insights.
  • Organized virtual Gastrointestinal Advisory Board to foster data sharing among global KOLs.
  • Increased efficiency for faster study cycle time, driving cross-functional team analysis and identifying root causes and recommendations to avoid delays.
Aug 2016 - Aug 2021
Frankfurt am Main, Germany

Global Medical Affairs Director - Erbitux mCRC Indication Lead, 2018–2021; Co-Lead, 2016–2018

Merck KGaA

Position summary
Global Medical Affairs Director - Erbitux mCRC Indication Lead, 2018–2021; Co-Lead, 2016–2018 at Merck KGaA
Industries
Biotechnology
Pharmaceutical
Business areas
Product Development
Project Management
Research and Development
Strategy

→ MEDICAL EXCELLENCE: OVERSAW GLOBAL MEDICAL AFFAIRS DECISION BOARD, DATA MAPPING, & LIFE CYCLE MANAGEMENT

  • Structured Global Medical Affairs approach for meaningful studies, research impact, and global medical decision alignment.
  • Chaired Global Medical Affairs Decision Board (Legal, Regulatory, Clinical Development, Statistician, HEOR, and other Leaders) to streamline approvals.
  • Directed Data Generation, Life Cycle Management, Phase IV study coordination, Advisory Board meetings, and materials creation for MSLs.
  • Led Medical Affairs, Marketing, Market Access / HEOR, and Commercial country leaders in new drug combination launch preparation.
  • Maintained engagement among Healthcare and Patient Advocacy Groups.

→ LIFE CYCLE TRENDS, REAL-WORLD DATA, & GLOBAL MEDICAL DECISION ALIGNMENT ACHIEVEMENTS

  • Identified Life Cycle Management trends by mapping data from ISTs; optimized IST strategy and generated valuable data in BRAF-mt.
  • Worked with In-Vitro Diagnostics companies to provide Liquid Biopsy test for key decisions in Life Cycle Management.
  • Organized ACTivate GI Ad Board meetings, including virtual communications platforms.
  • Partnered with Regulatory Affairs to represent Medical Affairs on drug labelling documentation.
  • Illuminated Real-World Data discoveries from Insurance claims database, with findings presented in specialist journal and congresses (HEOR).
  • Produced new insights by examining indication role in neuropathic pain (Proof-of-Concept, Clinical Development), working with investigators.
Oct 2013 - Jul 2016
Frankfurt am Main, Germany

Global Medical Affairs Director - Erbitux Life Cycle Management and Liquid Biopsies Lead

Merck KGaA

Position summary
Global Medical Affairs Director - Erbitux Life Cycle Management and Liquid Biopsies Lead at Merck KGaA
Industries
Pharmaceutical
Business areas
Operations
Project Management
Research and Development

→ LIQUID BIOPSY TESTING FOR REAL-WORLD BIOMARKER DATA

  • Generated insights into global biomarker testing practices by leading cross-functional Clinical Operations, Drug Safety, and HEOR teams to analyze Phase IV company-sponsored study.
  • Forged field relations with country Medical Science Liaisons; created scientific congress training materials with updated content.
  • Managed targeted therapy-immunotherapy Clinical Development (Phase I & II) - expanding treatment possibilities by advancing research using structured approach.
Jan 2012 - Sep 2013
France

Medical Affairs Director Oncology Europe

Teva Europe

Position summary
Medical Affairs Director Oncology Europe at Teva Europe
Industries
Healthcare
Pharmaceutical
Business areas
Project Management
Research and Development
Strategy

→ MEDICAL EXCELLENCE, STRATEGIC MEDICAL AFFAIRS PLANNING, M&A INTEGRATION, & COUNTRY AFFILIATE OVERSIGHT

  • Managed European Phase IV program in metastatic Breast Cancer and Supportive Care, leading cross-functional team including CROs, Drug Safety, Biostatistics, and Medical Writing leaders, line management reports, and 27 dotted-line country reports; developed budgets.
  • Organized European Advisory Boards and Congress Satellite Symposia.
  • Administered Medical Affairs for Oncology and Hematologic Malignancies, Biologics, and Biosimilars; produced and executed strategic Medical Affairs plan.

→ EUROPEAN LAUNCH READINESS & POST-M&A TEAM & PROGRAM INTEGRATION ACHIEVEMENTS

  • Coordinated medical launch preparation for new oncology supportive care product, ensuring medical support and alignment among cross-functional teams (Market Access, Legal, Regulatory, Clinical Development, other Leaders) and aggressive timelines.
  • Preserved productivity and strong morale by leading team members through acquisition and restructuring.
  • Cultivated and managed European KOL network; organized European Advisory Boards and Congress Satellite Symposia, including agendas and speaker selection.
Aug 2010 - Dec 2011
France

Associate Director Medical Affairs Oncology Europe

Cephalon, a Teva Group Member

Position summary
Associate Director Medical Affairs Oncology Europe at Cephalon, a Teva Group Member
Industries
Pharmaceutical
Business areas
Operations
Project Management
Research and Development

→ MEDICAL EXCELLENCE: EUROPEAN KOL NETWORK, ADVISORY BOARDS, & CONGRESS SYMPOSIA FOR BREAST CANCER PROGRAM

  • Managed Medical Affairs for Oncology and Hematologic Malignancies and Invasive Fungal Infections (including European Phase IV program in metastatic Breast Cancer and oversight of cross-functional CRO, Drug Safety, Biostatistics, and Medical Writing leaders).
  • Developed European KOL network.
  • Organized European Advisory Boards and Congress Satellite Symposia.
  • Oversaw up to 23 team and cross-functional reports, plus dotted-line country experts.
Sep 2008 - Jul 2010

Medical Project Manager Hemato-Oncology

Genzyme

Position summary
Medical Project Manager Hemato-Oncology at Genzyme
Industries
Biotechnology
Pharmaceutical
Business areas
Project Management
Research and Development

→ CLINICAL RESEARCH, MULTIPLE IST LAUNCHES, & SALES FORCE MEDICAL TRAINING

  • Drove 6 IST launches by heading Clinical Research, implementing company-sponsored Phase III study (Clinical Development), and managing French Phase I and II ISTs.
  • Built and managed French Key Opinion Leader relationships.
  • Led first Genzyme French Chronic Lymphocytic Leukaemia Advisory Board; organized local symposia.
  • Led Sales Force Medical Training with Marketing team; facilitated onboarding.
Nov 2006 - Aug 2008

Medical Advisor Anti-Infectives & HIV; Deputy Head Medical Affairs / Deputy Medical Advisor Oncology

Pfizer

Position summary
Medical Advisor Anti-Infectives & HIV; Deputy Head Medical Affairs / Deputy Medical Advisor Oncology at Pfizer
Industries
Pharmaceutical
Business areas
Product Development
Project Management
Research and Development

→ HIV PRODUCT LAUNCH; OVERSAW INFECTIOUS DISEASE ADVISORY BOARD AND FIRST SWISS HIV ADVISORY BOARD

  • Oversaw company-sponsored Phase III studies (Clinical Development), managed Swiss ISTs in Clinical Research, and built Swiss KOL network.
  • Managed Medical Information in Antifungals and Antibacterials and HIV.
Oct 2002 - Oct 2006

Medical Advisor Cardiovascular & Metabolism / Arthritis, Bones, & Hormone Replacement Therapies

Novartis Pharma Schweiz

Position summary
Medical Advisor Cardiovascular & Metabolism / Arthritis, Bones, & Hormone Replacement Therapies at Novartis Pharma Schweiz
Industries
Pharmaceutical
Business areas
Marketing
Research and Development
Sales

→ IMPLEMENTATION FOR COMPANY SPONSORED PHASE III CLINICAL RESEARCH STUDIES

  • Engaged, developed, and managed Swiss KOL network, supporting research studies (Clinical Development) for Type II Diabetes, Hypertension, Osteoarthritis and Osteoporosis.
  • Led Sales Team training with Marketing Team; facilitated new collaborator onboarding.
Oct 1997 - Sep 2002
Switzerland

Resident and Senior Resident in Internal Medicine and General Surgery

Various Regional and University Medical Hospitals

Position summary
Resident and Senior Resident in Internal Medicine and General Surgery at Various Regional and University Medical Hospitals
Industries
Healthcare

→ INTERNAL MEDICINE & GENERAL SURGERY: ENDOCRINOLOGY, RENAL DISEASES, ONCOLOGY / HAEMATOLOGY, ER, INTENSIVE CARE, DERMATOLOGY & IMMUNOLOGY, PLUS DIGESTIVE, TRAUMA / ORTHOPAEDIC, & UROLOGICAL SURGERY

Industry experience

See where this freelancer has spent most of their professional time.

Experienced in Pharmaceutical, Healthcare, and Biotechnology.

Pharmaceutical
Healthcare
Biotechnology
Profile match chart

Business area experience

See which departments and functions this freelancer has contributed to most.

Experienced in Research and Development, Project Management, Strategy, Operations, Product Development, and Marketing.

Research and Development
Project Management
Strategy
Operations
Product Development
Marketing
Profile match chart

Summary

Swiss-trained physician and independent Medical Affairs & Clinical Development Consultant with 20+ years of international Pharma and Biotech experience across global, European and country-level roles in Germany, France and Switzerland. Hands-on expertise in Medical Affairs strategy, clinical development, Real-World Evidence and evidence generation, Phase III/IV studies, Investigator Sponsored Trials, launch readiness and lifecycle management. Experienced in the development and revision of SOPs and medical processes at country, European and global level, both as team member and team lead. Strong track record leading cross-functional initiatives involving Clinical Operations, Drug Safety, Regulatory, HEOR/Market Access, Biostatistics, CROs and Medical Writing. Deep therapeutic expertise in Oncology, Haematology and Rare Diseases, supported by five years of clinical practice in Internal Medicine and General Surgery.

Skills

  • Medical Affairs & Medical Strategy

  • Rwe/Rwd, Nis & Phase Iv

  • Sop & Process Development

  • Clinical Development & Ists

  • Evidence Generation

  • Launch Readiness & Lifecycle Management

  • Scientific & Stakeholder Engagement

  • Oncology (Breast & Gi Cancers)

  • Haematology (Aml, Cll & Cml)

  • Rare Diseases

  • Internal Medicine

Languages

German
Native
English
Native
French
Native
Italian
Advanced

Education

University of Basel

University Professional of Advanced Studies in Pharmaceutical Medicine · Pharmaceutical Medicine · Basel, Switzerland

University of Geneva

Federal Diploma in Medicine · Medicine · Geneva, Switzerland

Certifications & licenses

AI Governance, Professional Certificate

The Corporate Governance Institute

Healthcare Transformation; AI in Healthcare; Leading Digital Transformation in Healthcare, Advanced Certificate

Harvard Medical School, Executive Education

Specialist in Pharmaceutical Medicine & General Medical Practitioner, Swiss Federal Postgraduate Diplomas

FMH (Swiss Medical Association)

Statistics

Experience

Total positions 10
Experience in Pharmaceutical 24 y
Avg length 2 y 10 m
Longest experience 5 y

Global experience

Countries worked in 3 (Germany, France, Switzerland)
Primary country Germany

Expertise

Recent roles Founder | Senior Clinical & AI Strategy Advisor to PE/VC & Boards, Global Medical Lead - Knowledge Management Capabilities Development - GMA Oncology, Global Medical Affairs Director - Erbitux mCRC Indication Lead, 2018–2021; Co-Lead, 2016–2018
Main industries Pharmaceutical, Healthcare, Biotechnology
Main business areas Research and Development, Project Management, Strategy

Qualifications

Highest degree Bachelor
Certifications earned 3

Profile

Member since
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Frequently asked questions

Have questions? Find more information here.

Philippe is based in Bad Homburg, Germany.

Philippe speaks the following languages: German (Native), English (Native), French (Native), Italian (Advanced).

Philippe has at least 29 years of experience. During this time, Philippe has worked in at least 10 different roles and for 8 different companies. The average length of individual experience is 3 years and 11 months. Note that Philippe may not have shared all experience and actually has more experience.

Based on recent experience, Philippe would be well-suited for roles such as: Founder | Senior Clinical & AI Strategy Advisor to PE/VC & Boards, Global Medical Lead - Knowledge Management Capabilities Development - GMA Oncology, Global Medical Affairs Director - Erbitux mCRC Indication Lead, 2018–2021; Co-Lead, 2016–2018.

Philippe's most recent position is Founder | Senior Clinical & AI Strategy Advisor to PE/VC & Boards at Nexevan Advisory.

In recent years, Philippe has worked for Nexevan Advisory and Merck KGaA.

Philippe is most experienced in industries like Pharmaceutical, Healthcare, and Biotechnology.

Philippe is most experienced in business areas like Research and Development, Project Management, and Strategy. Philippe also has some experience in Operations, Product Development, and Marketing.

Philippe has recently worked in industries like Healthcare, Pharmaceutical, and Biotechnology.

Philippe has recently worked in business areas like Strategy, Operations, and Project Management.

Philippe holds a Bachelor in Pharmaceutical Medicine from University of Basel.

Philippe has 3 certificates. These include: AI Governance, Professional Certificate, Healthcare Transformation; AI in Healthcare; Leading Digital Transformation in Healthcare, Advanced Certificate, Specialist in Pharmaceutical Medicine & General Medical Practitioner, and Swiss Federal Postgraduate Diplomas.

Philippe is immediately available for suitable projects.

Daily rate distribution

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<€800 €800-​960 €960-​1120 €1120-​1280 €1280+

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Daily rate avg. 941 €

The average daily rate is the mean of all daily rates from recent contracts of comparable freelancers on our platform.

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Median rate 932 €

The median daily rate is the middle value of all daily rates — half of comparable freelancers charge less, half charge more. Unlike the average, it is barely affected by outliers.

Calculated based on our freelancers’ daily rates as of 4 Sep 2026. Actual rates may vary depending on seniority level, experience, skill specialization, project complexity, and engagement length.