BrightOwl Loader Loading

Summary

Clinical research professional with 13 years experience in CRO, pharmaceutical and biotech industries and a passion for oncology.

Experiences

Current Experience

  • Associate director project management
    Since April 2015

Past Experience

  • Clinical Project Manager (CPM)
    August 2012 --- March 2015
    Managing of early phase clincial trials in oncology from protocol development to CSR finalization. Overseeing different vendors and project budget.

  • Clinical Project Manager/Clinical Operations Lead
    September 2008 --- July 2012
    country management of oncology trials; identification of study sites, contract management, budget calculation, management of CRA teams, liason with internal departments and external vendors

  • Clinical Operations Lead
    January 2008 --- January 2012

  • Clinical Project Manager (CPM)
    January 2007 --- August 2008
    Management of international oncology trials: support business development team, budget management, management of CRA teams, liason with internal departments and external vendors, main contact for client

  • Clinical Project Manager (CPM)
    January 2005 --- January 2007
    Management of international oncology trials: management of CRA teams, liason with internal departments, external vendors and clients

  • CRA/Project Manager
    September 2002 --- January 2005
    Monitoring of Oncoclgy Trials Management of Oncolgy Trials: main contact for sponsor and external vendors, manage CRA teams, liasion with internal departments Head of Office: personnel development

  • Postdoctoral fellow
    January 2000 --- January 2002

Knowledge

LinkedIn Assessment :
CROClinical trial managementCTMSEDCBiotechnology IndustryClinical monitoringICH-GCPClinical trialsoncologyPharmaceutical IndustryProject ManagementClinical DevelopmentClinical operationsClinical researchDrug DevelopmentClinical Trial OversightKlinische StudienKlinischer BetriebKlinische EntwicklungKlinische ForschungOnkologiePharmaindustrieKlinische ÜberwachungGCPGute klinische PraxisProjektmanagementProtocolClinical trialsProtokoll

Education

  • PhD in Chemie from Ruprecht-Karls-Universität Heidelberg in 2000
  • PhD in Chemie from Technische Universität Kaiserslautern in 2000
  • Diplom in Chemie from Universität des Saarlandes in 1996

Languages

BrightOwl Assessment:
Self Assessment:
German
Native
English
Professional Proficiency

Work Preferences

  • Notice Period:
    13 weeks
  • Locations I am interested in:
    Niedersachsen, Germany Nordrhein-Westfalen, Germany
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position :    75-100% FTE
  • International:
    Yes

Area / Region

Germany

Others

Driving License
  • No