Clinical Research Associate - Remote - Sponsor Dedicated
ICON plc
Vienna, Austria
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Clinical trial monitoring experience
Ich-gcp guidelines knowledge
Patient safety compliance
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ICON plc is seeking a Clinical Research Associate (CRA I) for a remote position dedicated to a sponsor, emphasizing collaboration and high-quality outcomes in clinical trial operations. The role requires relevant clinical trial monitoring experience, strong communication skills, and a willingness to travel.
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Job Summary
Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.
Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.
In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance.
Matching Summary
Match Score: 75
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ICON plc is seeking a Clinical Research Associate (CRA I) for a remote position dedicated to a sponsor, emphasizing collaboration and high-quality outcomes in clinical trial operations. The role requires relevant clinical trial monitoring experience, strong communication skills, and a willingness to travel.
**
Skills & Requirements
Must-have
Clinical trial monitoring experience
ICH-GCP guidelines knowledge
Patient safety compliance
Sponsor generated queries
Study documentation review
Nice-to-have
Collaborative stakeholder relationships
Timely query resolution
Fostering inclusive environment
Key Requirements
University degree in medicine, science, or equivalent
Excellent written and verbal communication in English