Clinical Research Coordinator-French-Dutch and English Speaker > IQVIA > Joboolo BE :
Company : IQVIA Location : Zaventem Flanders From : Talent BE
g., patient diaries, instructions) Document proper destruction of clinical supplies. Prepare Investigator trial file binders Execute eTMF Quality Control Plan Obtain translations of documents In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions Obtain, track and update study insurance certificates Support preparation of submission package for IRB/ERC and support regulatory agencies submissions. Publish study results for GCTO and RA where required per local legislation Your ProfileBachelor Degree in Administration or similar field.At least 3 -5 years of experience in a clinical environment as a CTA, medical assistant.French and Dutch and English Proficient Level.
Belgium Based.GCP knowledge,ETMF, CTMS professional usage.
Microsoft Office user.Hybrid role.What you can expect:
Resources that promote your career growthLeaders that support flexible work schedulesPrograms to help you build your therapeutic knowledgeExcellent working environment in a stabile, international, reputable companyAttractive benefits packageIQVIA is a leading global provider of advanced analytics, technology solutions and clinicalresearch services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
