
Clinical Data Scientist
4 days ago
As a Data Management Expert, you will be responsible for overseeing clinical data management activities across assigned clinical trials. Your primary objective is to ensure high-quality data acquisition, database design, and data integrity.
The ideal candidate will possess strong knowledge of EDC systems, clinical trial processes, and regulatory compliance (ICH-GCP). Additionally, experience in Risk-Based Monitoring (RBM), data cleaning, and data visualization tools is highly desirable.
Key Responsibilities:
- Oversee clinical data management activities to ensure timely, compliant, and efficient data management processes.
- Serve as a technical resource for Data Management (DM) and Risk-Based Monitoring (RBM) standards, tools, and reporting.
- Collaborate with cross-functional teams, external vendors, and internal stakeholders to maintain study-specific documentation in the Trial Master File (TMF).
- Support 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 analytical, communication, and problem-solving skills.
This role offers an excellent opportunity to leverage your expertise in clinical data management and make a meaningful contribution to the success of our projects.
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