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I am an experienced researcher with a strong training in the oncology and drug development field. Following my maternity break, I am now committed to transitioning into Regulatory Affairs.  In order to gain an entry into the field I have done a course from RAPS society and am knowledgeable in regulatory document creation,  EU rules, guidelines and practices. With strong multitasking and organizational experience of managing multiple projects, I bring a rigorous and methodical work attitude with strong attention to detail. With my demonstrated history of cross-functional and multicultural exposure in the scientific field Iintegrate quickly and effectively and work dynamically with diverse teams.



Past Experience


    August 2012 --- August 2017
    Drug Discovery

  • RESEARCH ASSISTANT Vienna, Austria

    June 2011 --- June 2012
    In Vitro

  • RESEARCH STUDENT Vienna, Austria

    September 2007 --- June 2012
    Data Analysis


Self Assessment :
AdaptabilityAttention to detailCollaborationCritical thinkingOrganization


Self Assessment :
Biochemistry Cell biology Scientific writingActions and modes of action of drugs in the human speciesAdverse Events (AE)Biological Drug DevelopmentBiomarkersBiopharmaceuticalsBiotechnologyTroubleshootingStudy protocolsScientific WritingScientific CommunicationsRegulatory submissionsProtein ExpressionPreclinical ResearchpharmacologyNew Drug Application (NDA)Molecular & Cellular BiologyMedical writing

Skills and Expertise

Self Assessment :
Guide students Interpret data Receptor Pharmacology Search literature on clinical trials Write protocolsAssist with experimentsAttend seminars, courses and meetings within and outside the companyBiomarker ResearchCell cultureCommunicationCoordinationData miningDesign scientific projects (in biology)Write papersWrite documentsWork collaboratively with the other members of the clinical research team Supervise techniciansReview data


  • Ph.D. in Cell Biology/Vascular Biology from Center for Physiology and Pharmacology, Medical University of Vienna in 2012
  • Master in Microbial Gene Technology and Molecular Biology from Madurai Kamaraj University, India in 2006
  • Bachelor in Biotechnology, Zoology, Chemistry from University of Kerala, India in 2004

Training and Certification

  • Regulatory Medical Writing in 2019 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Professional Proficiency

Work Preferences

  • Positions I am interested in:
    Assay Development Manager Regulatory Affairs Assistant Regulatory Affairs Consultant Regulatory Affairs Associate R&D manager Research Assistant
  • Work From Home:
    Yes, 0 to 3 days per week
  • Work Regime:
    Permanent position :    100% of a full time equivalent% FTE
    BrightOwl employee :    100% of a full time equivalent% FTE
  • International:

Area / Region

1410 Waterloo, Belgium


Driving License
  • No

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