CRA (M/W/D)
Tasks:
Clinical monitoring of current studies
Patient recruitment Follow-up
Study Preparation / Study Start-up
Site Contract Negotiation
Qualification & Initiation Visits
Submission processes, preferably in Germany
Supervision of studies
Preparation and filing of study documents
Monitoring visit reports and Follow-up
Qualification:
Completed studies in natural sciences
Several years of CRA experience
Experience in the field of vaccine and/or respiratory tract
Hands-on mentality, solution orientated
Business fluent in German & English
Requirements:
Start: asap
Duration: 24 months
Capacity: 5 days per week
Location: remote & onsite
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