
Norway Clinical Research Professional
2 days ago
The Clinical Research Associate position at IQVIA LLC offers a unique opportunity to work with a leading healthcare company and contribute to the success of clinical trials.
About the Role:
- Conduct site visits to monitor and manage study progress.
- Work closely with sites to develop and implement recruitment strategies.
- Evaluate the quality and integrity of study site practices related to protocol adherence and regulatory compliance.
- Manage the progression of studies through tracking regulatory submissions, recruitment and enrollment, CRF completion, and data query resolution.
Requirements:
- Bachelor's degree in a scientific discipline or healthcare preferred.
- At least 2 years of on-site monitoring experience.
- Good knowledge of clinical research regulatory requirements, including GCP and ICH guidelines.
- Strong therapeutic and protocol knowledge, as well as computer skills and communication skills.
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Clinical Research Professional
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