Clinical trial workflow
Understand how data moves through the lifecycle of a clinical study from collection to reporting.
Gain practical experience in clinical trial data workflows through live industry training, virtual internship, and hands-on case studies.
Students learn how clinical trial data is collected, cleaned, validated, and managed using industry workflows. The program covers clinical research fundamentals, data quality, documentation, and real case-based exercises aligned with common CDM practices.
Understand how data moves through the lifecycle of a clinical study from collection to reporting.
Learn the core processes behind case report forms, data cleaning, and data validation.
Work with structured data collection tools and understand the role of standardized forms.
Practice identifying issues, resolving discrepancies, and maintaining data integrity.
Build confidence in data handling practices, SOP awareness, and the documentation standards used in clinical research.
Complete a simulated clinical data management project involving CRFs, validation, discrepancy management, and reporting.
Every Nexxora cohort concludes with one mentor-guided capstone project designed to strengthen your portfolio, build practical experience, and prepare you for interviews.
Work through a simulated clinical trial data management process while learning how industry teams manage data quality, validation, and regulatory compliance.
Clinical Data portfolio project
GCP workflow exposure
Query management practice
Interview-ready experience
Clinical Data Associate
Clinical Data Coordinator
Clinical Operations Associate
Clinical Research Associate (Entry Level)
Healthcare Data Associate
Graduates receive a Nexxora cohort certificate tied to their completed projects, mentor review, and live learning record.
Training Certificate, Virtual Internship Certificate are awarded on completion of the program.
B.Pharm, M.Pharm, Pharm.D, biotechnology, life sciences, microbiology, biochemistry, and clinical research aspirants.
You will learn the clinical trial workflow, clinical data management, CRF and eCRF processes, data cleaning, query management, GCP basics, medical terminology, and documentation.
You will complete a simulated clinical data management project with validation, discrepancy management, and reporting elements.