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Experiences

Current Experience

  • Clinical Project Manager (CPM) Lithuania
    Since June 2013

Past Experience

  • Clinical Operations Lead Lithuania
    July 2011 --- June 2013

  • SCRA - CPM Lithuania
    November 2006 --- July 2011

  • SCRA Lithuania
    November 2005 --- November 2006

  • CRA-SCRA Latvia
    October 2001 --- November 2005

Skills and Expertise

Self Assessment :
Develop clinical trial protocols Develop protocols Build and manage the Trial Master File (TMF) Create SOPs Guide students Control data Interact with nurses Interact with physicians Monitor a clinical study Report data Search literature on clinical trialsAdminister logisticsAdjust processes Administer supply requestApprove consent documentsAdverse event reportingApprove monitoring reportsApprove Label Master SheetArchive study documents Design case record formsAssess site feasibilityAssess subject safetyApprove drug supply Assist study siteAssign activitiesAttend investigator meetingBuild CMC development planCalculate trial timelinesCollaborate with medical teamCoach clinical staffCollaborate with principal investigatorCollaborate with project teamCommunicate with sponsorCommunicate with investigatorCollect financial data from hospitalsbudgeting of R&D activitiesComplete study proceduresConduct monitor visits Interpret dataConduct site initiationConduct close-out visitsConduct the trial Lab scale batches

Education

  • Master in Occupational Therapy from Kaunas Medical University in 2001
  • Bachelor in Public Health from Kaunas Medical University in 2000

Languages

BrightOwl Assessment:
Self Assessment:
English
Full Proficiency
Lithuanian
Native
Russian
Native

Work Preferences

  • Positions I am interested in:
    Clinical Project Manager (CPM) Clinical Operations Manager
  • Work From Home:
    No
  • Work Regime:
    Permanent position :    100% FTE
    BrightOwl freelancer
    BrightOwl employee :    100% FTE
  • International:
    Yes

Area / Region

Lithuania

Others

Driving License
  • No