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Clinical Research Professional with 13 years experience in CRO, Pharmaceutical and biotech industries and a passion for oncology.


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 science)" rel="nofollow">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


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


  • 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


BrightOwl Assessment:
Self Assessment:
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:

Area / Region



Driving License
  • No

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