Experienced CRA - Denmark
IQVIA(7 months ago)
About this role
An Experienced Clinical Research Associate (CRA) based in Denmark supporting clinical trial oversight and ensuring studies meet protocol, regulatory, and sponsor standards. The role is field-focused and acts as a liaison between study sites and sponsor teams to facilitate accurate trial documentation and data integrity.
Required Skills
- Site Monitoring
- GCP
- ICH
- Protocol Knowledge
- Recruitment Planning
- Regulatory Submissions
- CRF Management
- TMF Maintenance
- Communication
- Time Management
+2 more
Qualifications
- Bachelor's Degree in Scientific Discipline
About IQVIA
iqvia.comIQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.
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