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My experience, skill and knowledge of Clinical Trials are thorough from more then 5 years working as Senior Clinical Research Associate (SCRA), Clinical Team Leader and Medical Director within CRO and pharma industry but also from 9 years experience as Certified Registered Physician with practical and documented knowledge in General Practitioner My strength: I am efficient, result driven, goal oriented, good at prioritizing tasks and supporting others to prioritize. I set an honor in reaching set targets and deadlines and constantly strive to improve and refine work processes with compliance and quality in mind.


Current Experience

  • Medical Director, Dermato-venereology, MD
    Since July 2011

    - Investigator or Subinvestigator for clinical studies – medical surveillance for protocol compliance - Scientific expertise related to feasibility research, data collection and interpretation - Medical review of study documents and clinical study data - Generates feasibility project specific documents - Leading and training the technical study team - Manage global clinical trials from study start-up to close-out - Ensure study conduct in accordance with appropriate SOPs, ICH/GCP Guidelines and local Regulations

Past Experience

  • General practitioner, GP
    January 2009 --- January 2011
    Occupational Medicine - evaluation, diagnose and treat occupational disease and injury

  • General practitioner, GP
    January 2008 --- January 2009
    Occupational Medicine - evaluation, diagnose and treat occupational disease and injury


Self Assessment :
Analytical thinkingAttention to detailCommunicativeCompetitivenessCoordinationCollaborationEfficiencyFlexibilityInnovative thinkingResult OrientedProactivity


Self Assessment :
Project ManagementClinical trial managementClinical monitoringDermatologyDrug Safety and PharmacovigilanceGCPEnglishGeneral practicePharmaceutical IndustrySenior Clinical Research AssociateColorectal surgery
LinkedIn Assessment :
MedicineHealthcareNegotiationProject ManagementNew Business DevelopmentStrategic PlanningClinical researchHealthcare ManagementHospitalsMedical EducationClinical trialsRegulatory submissionsCTMSGCPCROICH-GCPClinical DevelopmentPharmaceutical IndustryoncologyCancerProtocolPublic HealthInternal medicine

Skills and Expertise

Self Assessment :
Develop clinical trial protocols Develop protocols Control data Interact with physicians Monitor a clinical studyDevelop ICH/GCP compliant processesClinical data collectionComplete case report form (CRF)Design clinical trialEnsure good clinical practice (GCP)Manage Clinical Trial Management System (CTMS) Monitor a clinical studyMonitor clinical trials Clinical Research Associate


  • Bachelor’s Degree in Medicine from University of Medicine and Pharmacy Iuliu Hatieganu, Cluj Napoca, Romania in 2006
  • High School in Physics - Chemistry from Nicolae Balcescu National College, Braila, Romania in 1999

Training and Certification

  • Cambrige ESOL Level 2 certificate in Esol International Grade C Certification
  • Certificate in GCP Training Course based on ICH E6 - Investigator Certification
  • Residency - Family Medicine Certification
  • Resident physician in dermato-venereology Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Full Proficiency
Full Proficiency
Elementary Proficiency
Elementary Proficiency

Work Preferences

  • Notice Period:
    2 weeks
  • Locations I am interested in:
    Belgium Finland France Great Britain Luxembourg Netherlands Sweden Switzerland
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position
  • International:

Area / Region

Bucharest, Romania


Driving License
  • Yes