Study Assistant Specialist
Vor 6 Tagen
Job Summary:
We are seeking a highly skilled and detail-oriented Clinical Research Assistant to support our clinical study in Hamburg. As a key member of our team, you will be responsible for coordinating research studies, ensuring the well-being of volunteers, and maintaining study documents up to date.
Key Responsibilities:
- Coordinate research studies, including scheduling, data collection, and reporting.
- Ensure the well-being of volunteers, including providing support and guidance as needed.
- Maintain study documents, including case report forms, informed consent forms, and study protocols.
- Collaborate with cross-functional teams, including research scientists, clinicians, and data analysts.
- Develop and maintain knowledge of clinical studies, including regulatory requirements and industry standards.
Requirements:
- At least one year of relevant experience in clinical research.
- Knowledge of clinical studies, including regulatory requirements and industry standards.
- Strong IT skills, including proficiency in Microsoft Office and data management software.
About IQVIA:
IQVIA is a global provider of advanced analytics and clinical research services. We are committed to creating a healthier world through our work in clinical research, data analytics, and healthcare technology.
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