Successful clinical development. Period.
Aktualisiert am 29.10.2025
Profil
Freiberufler / Selbstständiger
Remote-Arbeit
Verfügbar ab: 01.11.2025
Verfügbar zu: 50%
davon vor Ort: 10%
Clinical Development
Regulatory Affairs
Medical Monitoring
GCP Compliance
Good Pharmacovigilance Practice
COPD Development
COPD Treatment
New COPD Treatments
Aerosol Medicine
Aerosol Treatment
German
Muttersprache
English
Verhandlungssicher
Danish
Fortgeschritten
French
Grundkenntnisse

Einsatzorte

Einsatzorte

Hamburg (+150km) Flensburg (+100km) Husum, Nordsee (+100km) Tønder (+50km)
Deutschland
möglich

Projekte

Projekte

3 years 4 months
2022-08 - now

ACliRA Consulting ApS

Administrerende direktør
Administrerende direktør
  • Consulting for different pharma and medical device companies in clinical development for respiratory and infectious diseases as well as sleep medicine
  • Participation in due diligence activities, assessment of assets for various pharmaceutical and medical device businesses
  • Professional presentations and talks in clinical development
  • Creating contacts to key opinion leaders and study sites for participation in clinical trials
  • Safety review and medical monitoring of early and late-stage clinical trials in various EDC environments
Various Customers
5 years 11 months
2020-01 - now

Consulting for different pharma and medical device companies

Managing Director
Managing Director
  • Consulting for different pharma and medical device companies
  • Participation in due diligence activities, assessment of assets for various pharmaceutical and medical device businesses
  • Professional presentations and talks in clinical development
ACliRA Consulting GmbH i.L., Gemünden, Germany (in Liquidation)
3 years
2020-01 - 2022-12

Responsible for overall development strategy

Chief Medical Officer
Chief Medical Officer
  • Responsible for overall development strategy of AspiAir
  • Overseeing and managing clinical development in different indication for inhaled medicines
  • Presenting development strategy and results of development to partners and investors
  • Leading the clinical development team
AspiAir GmbH, Gemünden/Wohra, Germany (part time)
5 years
2015-05 - 2020-04

Responsible for overall development strategy

Consulting Chief Medical Officer
Consulting Chief Medical Officer
  • Responsible for overall development strategy of ATRIVA
  • Overseeing and managing clinical development in infectious diseases (Influenza, RSV, Hantavirus)
  • Presenting development strategy and results of development to partners and investors
  • Leading the clinical development team
ATRIVA Therapeutics GmbH, Tübingen (Germany)
3 years 9 months
2016-04 - 2019-12

Patient care

Chief Medical Officer
Chief Medical Officer
Ventaleon GmbH, Gemünden/Wohra, Germany (part time)
9 years
2011-01 - 2019-12

Self-Employment

Independent Consultant
Independent Consultant
6 years 7 months
2009-09 - 2016-03

various medical activities

  • Assoc. Dir. Pharmacovigilance and EU-QPPV (since 04/2014)
  • Director Clinical Development and Drug Safety, EU-QPPV(until 03/2014)
Vectura GmbH, Gemünden/Wohra, Germany (part time)(former Activaero GmbH, Gemünden/Wohra until 03/2014)
7 years
2005-05 - 2012-04

Residency

University Hospital Gießen and Marburg GmbH, Marburg/ Dept. Internal Medicine with focus Pulmonology

Aus- und Weiterbildung

Aus- und Weiterbildung

1 year 11 months
2005-05 - 2007-03

Human Medicine

Doctor of Human Medicine (Dr. med.), Philipps-University Marburg
Doctor of Human Medicine (Dr. med.)
Philipps-University Marburg
7 years 3 months
1998-02 - 2005-04

Human Medicine

Medical Doctor (M.D.), Philipps-University Marburg
Medical Doctor (M.D.)
Philipps-University Marburg

Position

Position

Managing Director of my own Consulting Company, working with different clients worldwide in clinical development / regulatory affairs / medical monitoring.

Kompetenzen

Kompetenzen

Top-Skills

Clinical Development Regulatory Affairs Medical Monitoring GCP Compliance Good Pharmacovigilance Practice COPD Development COPD Treatment New COPD Treatments Aerosol Medicine Aerosol Treatment

Produkte / Standards / Erfahrungen / Methoden

Profile
Working in the area of clinical development for more than 20 years, I can support your development project to become a success story, in early as well as late phase. My background with a medical education from the Universities of Marburg and Baltimore, as well as residency time in pulmonology and interdisciplinary sleep medicine laid the foundation for a successful career in clinical development. My extensive working experience in the pharmaceutical and medical device industry in senior management positions ensures that the overall picture of any clinical development remains a key focus. Therefore, my support will go beyond just study conduct, but incorporates strategic planning, SWOT analyses, due diligence assessments and safety reviews/medical monitoring. My expertise can help you achieve the goals for a timely and cost-efficient clinical development.

IT
MS-Office (including admin roles), Mac OSX, Windows 10/11, various EDC environments (Clinspark, Medrio, Castor, QCTMS)

Work periods abroad
07/2001 ? 10/2001
Johns-Hopkins University, Baltimore, MD, USA
Scientific Internship

04/2014 ? 03/2016
Regular attendance at international project meetings of mother company Vectura Group plc. in Chippenham/Wiltshire, UK

Scientific Experience
2020 - today
Independent Medical Expert 
 GCP-Service International Ltd. & Co. KG, Bremen, Germany

2013 - today
Scientific Advisory Board of the Journal ?Atemwegs- und Lungenkrankheiten? Dustri Verlag

2007 - today
Reviewer for scientific journals
  • Biomed. Technik (Berlin)
  • IEEE Transactions on Information Technology in Biomedicine
  • IEEE Transactions on Biomedical Engineering
  • Journal of Sleep Research; Physiological Measurement
  • Somnology; Pulmonary Medicine

Branchen

Branchen

Larger and smaller pharma companies in the area of clinical development / regulatory affairs / medical monitoring.

Einsatzorte

Einsatzorte

Hamburg (+150km) Flensburg (+100km) Husum, Nordsee (+100km) Tønder (+50km)
Deutschland
möglich

Projekte

Projekte

3 years 4 months
2022-08 - now

ACliRA Consulting ApS

Administrerende direktør
Administrerende direktør
  • Consulting for different pharma and medical device companies in clinical development for respiratory and infectious diseases as well as sleep medicine
  • Participation in due diligence activities, assessment of assets for various pharmaceutical and medical device businesses
  • Professional presentations and talks in clinical development
  • Creating contacts to key opinion leaders and study sites for participation in clinical trials
  • Safety review and medical monitoring of early and late-stage clinical trials in various EDC environments
Various Customers
5 years 11 months
2020-01 - now

Consulting for different pharma and medical device companies

Managing Director
Managing Director
  • Consulting for different pharma and medical device companies
  • Participation in due diligence activities, assessment of assets for various pharmaceutical and medical device businesses
  • Professional presentations and talks in clinical development
ACliRA Consulting GmbH i.L., Gemünden, Germany (in Liquidation)
3 years
2020-01 - 2022-12

Responsible for overall development strategy

Chief Medical Officer
Chief Medical Officer
  • Responsible for overall development strategy of AspiAir
  • Overseeing and managing clinical development in different indication for inhaled medicines
  • Presenting development strategy and results of development to partners and investors
  • Leading the clinical development team
AspiAir GmbH, Gemünden/Wohra, Germany (part time)
5 years
2015-05 - 2020-04

Responsible for overall development strategy

Consulting Chief Medical Officer
Consulting Chief Medical Officer
  • Responsible for overall development strategy of ATRIVA
  • Overseeing and managing clinical development in infectious diseases (Influenza, RSV, Hantavirus)
  • Presenting development strategy and results of development to partners and investors
  • Leading the clinical development team
ATRIVA Therapeutics GmbH, Tübingen (Germany)
3 years 9 months
2016-04 - 2019-12

Patient care

Chief Medical Officer
Chief Medical Officer
Ventaleon GmbH, Gemünden/Wohra, Germany (part time)
9 years
2011-01 - 2019-12

Self-Employment

Independent Consultant
Independent Consultant
6 years 7 months
2009-09 - 2016-03

various medical activities

  • Assoc. Dir. Pharmacovigilance and EU-QPPV (since 04/2014)
  • Director Clinical Development and Drug Safety, EU-QPPV(until 03/2014)
Vectura GmbH, Gemünden/Wohra, Germany (part time)(former Activaero GmbH, Gemünden/Wohra until 03/2014)
7 years
2005-05 - 2012-04

Residency

University Hospital Gießen and Marburg GmbH, Marburg/ Dept. Internal Medicine with focus Pulmonology

Aus- und Weiterbildung

Aus- und Weiterbildung

1 year 11 months
2005-05 - 2007-03

Human Medicine

Doctor of Human Medicine (Dr. med.), Philipps-University Marburg
Doctor of Human Medicine (Dr. med.)
Philipps-University Marburg
7 years 3 months
1998-02 - 2005-04

Human Medicine

Medical Doctor (M.D.), Philipps-University Marburg
Medical Doctor (M.D.)
Philipps-University Marburg

Position

Position

Managing Director of my own Consulting Company, working with different clients worldwide in clinical development / regulatory affairs / medical monitoring.

Kompetenzen

Kompetenzen

Top-Skills

Clinical Development Regulatory Affairs Medical Monitoring GCP Compliance Good Pharmacovigilance Practice COPD Development COPD Treatment New COPD Treatments Aerosol Medicine Aerosol Treatment

Produkte / Standards / Erfahrungen / Methoden

Profile
Working in the area of clinical development for more than 20 years, I can support your development project to become a success story, in early as well as late phase. My background with a medical education from the Universities of Marburg and Baltimore, as well as residency time in pulmonology and interdisciplinary sleep medicine laid the foundation for a successful career in clinical development. My extensive working experience in the pharmaceutical and medical device industry in senior management positions ensures that the overall picture of any clinical development remains a key focus. Therefore, my support will go beyond just study conduct, but incorporates strategic planning, SWOT analyses, due diligence assessments and safety reviews/medical monitoring. My expertise can help you achieve the goals for a timely and cost-efficient clinical development.

IT
MS-Office (including admin roles), Mac OSX, Windows 10/11, various EDC environments (Clinspark, Medrio, Castor, QCTMS)

Work periods abroad
07/2001 ? 10/2001
Johns-Hopkins University, Baltimore, MD, USA
Scientific Internship

04/2014 ? 03/2016
Regular attendance at international project meetings of mother company Vectura Group plc. in Chippenham/Wiltshire, UK

Scientific Experience
2020 - today
Independent Medical Expert 
 GCP-Service International Ltd. & Co. KG, Bremen, Germany

2013 - today
Scientific Advisory Board of the Journal ?Atemwegs- und Lungenkrankheiten? Dustri Verlag

2007 - today
Reviewer for scientific journals
  • Biomed. Technik (Berlin)
  • IEEE Transactions on Information Technology in Biomedicine
  • IEEE Transactions on Biomedical Engineering
  • Journal of Sleep Research; Physiological Measurement
  • Somnology; Pulmonary Medicine

Branchen

Branchen

Larger and smaller pharma companies in the area of clinical development / regulatory affairs / medical monitoring.

Vertrauen Sie auf Randstad

Im Bereich Freelancing
Im Bereich Arbeitnehmerüberlassung / Personalvermittlung

Fragen?

Rufen Sie uns an +49 89 500316-300 oder schreiben Sie uns:

Das Freelancer-Portal

Direktester geht's nicht! Ganz einfach Freelancer finden und direkt Kontakt aufnehmen.