BrightOwl Loader Loading

Summary

ambitious, enthusiastic and eager to learn Clinical Research Coordinator, wants to continue to grow within the field of clinical research. has experience in performing several different clinical studies. is well able to work in a team and can adjust and adapt in changing cultures and working environments. has excellent Communication Skills, in written and spoken English and dutch. is independent, precise and a real 'troubleshooter’. has learned to work according to the Good Clinical Practice guidelines, by the (co) establishing of various studies. can motivate both children as well as adults in a natural way. has perseverance and can really ‘get into’ at a topic under the incentive that giving up is not an option . 

Experiences

Current Experience

  • Clinical Research Coordinator

    Velp, Nederland
    Since August 2013

     

    responsible for the proper implementation of, and Compliance with, several research protocols in the field of cardiovascular disease. setting up Phase II - iv studies from initiation until close-out. responsible for the right transcription of source documents into eCRF’s and for resolving any queries. caused by my critical view being an important Member in the quality committee of andromed in creating and refreshing SOP’s. responsible for distributing of study documents to the right colleagues (pi, sub-i or research Nurse).

    as a Research Coordinator thé contact point on behalf of the site in velp for Pharmaceutical companies, but also for patients. in this way, the crucial link link between theory and practice. 

     

    Responsible for the proper implementation of, and compliance with, several research protocols in the field of cardiovascular disease. Setting up phase II - IV studies from initiation until close-out. Responsible for the right transcription of source documents into eCRF’s and for resolving any queries. Caused by my critical view being an important member in the quality committee of Andromed in creating and refreshing SOP’s. Responsible for distributing of study documents to the right colleagues (PI, SUB-I or research nurse).

    As a research coordinator thé contact point on behalf of the site in Velp for pharmaceutical companies, but also for patients. In this way, the crucial link link between theory and practice. 

Past Experience

  • Research Assistant Amsterdam, Nederland

    November 2012 --- December 2012

     

    setting up and implementing the design of a new treadmill science)" rel="nofollow">Protocol for children with disabilities. this involved collection of norm scores for a new treadmill science)" rel="nofollow">Protocol in children between 6 and 12 years. 

  • Research Assistant ABCD study Amsterdam

    September 2012 --- October 2012

     

    assisted in performing tests in the olympic stadium in amsterdam in children between 8 and 10 years. these tests involved fitness and muscle strength measurements. 

  • Student Researcher Oxford, Verenigd Koninkrijk

    February 2012 --- July 2012

     

    Research about physical fitness and strength in children. designed and setting up a Research plan. administrated various tests in children. analysed the data and written a thesis

Personality

Self Assessment :
AdaptabilitySelf-disciplineProblem solvingOrganizationInterest in knowledgeIndependenceFlexibilityEfficiencyCritical thinkingCoordinationCharmService oriented

Knowledge

Self Assessment :
Diabetes Scientific writingCardiovascular diseasesClinical researchClinical Study DesignClinical trial audits and inspectionsClinical trialsEnglishGCPGood Clinical Practice (GCP)ICH GCP guidelinesInformed Consent ProcessMicrosoft OfficePowerPointPhases of clinical development (phase I to IV)ProtocolScientific WritingScreen patientsSerious Adverse Event (SAE)SOPWriting Study Procedures and SOPs

Skills and Expertise

Self Assessment :
Create SOPs Interact with nurses Interact with physicians Monitor a clinical study Search literature on clinical trials Write papersAdverse event reporting

Education

  • Master in Movement Science from Maastricht University in 2012
  • Bachelor in Health Science from Maastricht University in 2011

Training and Certification

  • Emergency Response Officer in 2015 Certification
  • Good Clinical Practice in 2014 Certification

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
English
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Work From Home:
    Yes, 0 to 3 days per week
  • Work Regime:
    Permanent position :    80-100% FTE
    BrightOwl employee :    80-100% FTE
  • International:
    No

Publications

    Expert has 1 publications (Will be avalible with full profile)

Area / Region

Nijmegen, Nederland

Others

Driving License
  • Yes

Similar Candidates

Other Candidates in Netherlands

Other Candidates in Nijmegen

Other similar Candidates in Nijmegen

Other Candidates

Most Recent Searches

Most Famous Searches

You might also like