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The Clinical Data Science Programmer will develop and validate programming solutions for analyzing clinical trial data, ensuring data integrity and compliance.

The role involves developing and validating statistical programs for clinical trials, collaborating with teams on analysis, and mentoring junior programmers.

Develop and validate statistical programming code for clinical trial data analysis and reporting, ensuring data integrity and compliance with standards.

The Clinical Data Coordinator II will assist in managing eCRF, data validation, and study procedures, track study metrics, and resolve data issues.

The Senior Statistical Programmer analyzes clinical trial data, develops SAS programs, collaborates with biostatisticians, and ensures compliance with regulatory standards.

Lead the design, development, and validation of data science programming solutions for clinical trials, ensuring data accuracy and quality.

The Clinical System Designer II will design, implement, and optimize clinical systems used in clinical trials, ensuring compliance and user satisfaction while providing training and support.

Responsible for processing and reconciling invoices, handling payments, and managing documentation in compliance with statutory requirements.

The Accounts Receivable Associate will manage invoicing, ensure compliance with contracts, collaborate with Project Managers, and support month-end processes.

Discover and analyze clinical trials data while managing data reconciliation and resolving data issues in a fast-paced environment.