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2 days ago
Job Title: Clinical Data Specialist
Role OverviewAs a Clinical Data Specialist, you will be responsible for leading clinical data management activities across assigned clinical trials. Your primary objective will be to ensure high-quality data acquisition, database design, and data integrity.
Key Responsibilities:- Lead the development of data management plans and strategies to support clinical trials
- Collaborate with cross-functional teams to ensure timely, compliant, and efficient data management processes
- Act as a technical resource for Data Management (DM) and Risk-Based Monitoring (RBM) standards, tools, and reporting
- Support data cleaning, integrity monitoring, e-data processing, and database release according to SOPs and industry best practices
- 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
This position offers an exciting opportunity to make a meaningful impact on the success of our clinical trials. If you are passionate about data management and eager to contribute to the advancement of life-changing therapies, we encourage you to apply.
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