Clinical Trial Management Associate
IQVIA(12 days ago)
About this role
This role involves supporting clinical trial processes, including document management, site coordination, and administrative tasks in a pharmaceutical or CRO setting. It requires collaboration with teams to ensure regulatory compliance, proper documentation, and smooth site operations, contributing to the advancement of medical research.
Required Skills
- Microsoft Word
- Excel
- PowerPoint
- Clinical Research
- Regulatory Compliance
- Document Management
- Communication
- Health Sciences
- Pharmaceuticals
Qualifications
- Bachelors Degree in Pharmaceutical or related field
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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