
Senior Clinical Data Manager
1 day ago
As a seasoned professional, you will oversee clinical data management activities across assigned trials to ensure high-quality data acquisition, database design, and data integrity.
- You will serve as a technical expert for Data Management and Risk-Based Monitoring standards, tools, and reporting.
- Collaborating with cross-functional teams, external vendors, and internal stakeholders is crucial to achieve timely, compliant, and efficient data management processes.
- Maintaining study-specific documentation in the Trial Master File (TMF) is essential.
- Supporting data cleaning, integrity monitoring, e-data processing, and database release according to SOPs and industry best practices is key.
A Bachelor's or Master's degree in Life Sciences, Pharmacy, Clinical Research, or a related field is required. Minimum 3 years of experience in Clinical Data Management within the pharmaceutical or CRO industry is also necessary.
- Strong knowledge of EDC systems, clinical trial processes, and regulatory compliance (ICH-GCP) is essential.
- Experience in Risk-Based Monitoring, data cleaning, and data visualization tools is highly valued.
- Excellent analytical, communication, and problem-solving skills are required.
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