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Senior CRA

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Aline Vandermeeren
Recruiter



Aline Vandermeeren
Recruiter
+32 497 71 58 10


Description de l'emploi

As a Clinical Research Associate you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

  • Conduct and report SIV, RMV, COV onsite monitoring visits
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions
  • Prepare and particiapte on audits and inspections

Profil


  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in Oncology is a plus
  • Full working proficiency in English 
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel
  • Valid driver’s license

Postes vacants connexes

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Coordonnées de contact

Formation et expérience

Postes vacants connexes

Senior Research Associate


Site Identification Specialist (Feasibility)