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Kwai Tsing District, Hong Kong SAR China IQVIA Argentina Full timeQualificationsThe successful candidate will possess a Bachelor's Degree in Life Sciences or a related field and 1-3 years of clinical research experience.Additional qualifications include:Experience in a healthcare environment.Advanced knowledge within a specific discipline.
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Clinical Research Associate
1 week ago
Job Overview
- Ensure the integrity of clinical trials by monitoring and managing site activities in accordance with contracted scope, regulatory requirements, and study protocols.
- Develop and implement site recruitment strategies to meet project objectives.
- Evaluate site performance, address quality issues, and provide regular updates on study progress.
Key Responsibilities
- Perform site monitoring visits to ensure compliance with GCP and ICH guidelines.
- Collaborate with sites to adapt and track subject recruitment plans.
- Administer protocol training to assigned sites and establish regular communication channels.
- Manage case report form completion, data query generation, and resolution.
Qualifications
- Bachelor's Degree in a scientific discipline or healthcare preferred.
- At least 1 year of on-site monitoring experience.
- Good knowledge of clinical research regulations and therapeutic areas.
- Excellent communication and organizational skills.