
Scientific Lead
20 hours ago
The ideal candidate for this position will possess a strong background in clinical data management, as well as experience in leading trial activities.
This role requires excellent analytical, communication, and problem-solving skills. The successful candidate will ensure high-quality data acquisition, database design, and data integrity across assigned clinical trials.
Key Responsibilities:
- Data Management Lead: Ensure timely, compliant, and efficient data management processes.
- Tech Resource: Support Data Management (DM) and Risk-Based Monitoring (RBM) standards, tools, and reporting.
- Cross-Functional Collaboration: Work with external vendors and internal stakeholders to ensure seamless data management processes.
- Documentation Management: Maintain study-specific documentation in the Trial Master File (TMF).
- Data Support: Assist with data cleaning, integrity monitoring, e-data processing, and database release according to SOPs and industry best practices.
Qualifications:
- Bachelor's or Master's degree in Life Sciences, Pharmacy, Clinical Research, or related field.
- 3+ years of experience in Clinical Data Management within the pharmaceutical or CRO industry.
- Strong knowledge of EDC systems, clinical trial processes, and regulatory compliance (ICH-GCP).
- Experience in Risk-Based Monitoring (RBM), data cleaning, and data visualization tools.
- Excellent analytical, communication, and problem-solving skills.
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