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Cdm Summer Internship

Join CDM summer internships to gain hands-on experience in clinical data management, focusing on clinical trial data collection, database design, and data validation for ensuring data accuracy in regulatory submissions.

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CDM Summer Internships

Join CDM summer internships to gain hands-on experience in clinical data management, focusing on clinical trial data collection, database design, and data validation for ensuring data accuracy in regulatory submissions.
In 200+ Other Fields

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Proj / Publications
Back to All Summer Internships.
Join our Cdm Publication Projects and earn co-authorship in the articles that will be published in Scopus Indexed or Science Citation Index (SCI) journals.

Focused Areas under Cdm Summer Internship

  1. Clinical data management systems in clinical trials
  2. Database design and implementation for clinical studies
  3. Electronic data capture systems for clinical trials
  4. Data validation and cleaning in clinical research
  5. CDISC standards implementation in clinical data management
  6. Clinical trial data collection and management protocols
  7. Data integrity and regulatory compliance in clinical trials
  8. Adverse event data management and reporting
  9. Electronic case report form (eCRF) design and implementation
  10. Data query management and resolution
  11. Quality assurance and control in clinical data management
  12. Clinical trial metadata management systems
  13. Database locking and freezing for clinical studies
  14. Database design for pharmacovigilance data
  15. Integration of data management systems with regulatory bodies
  16. Implementation of electronic trial master files (eTMF)
  17. Data extraction and reporting for clinical trials
  18. Risk-based monitoring in clinical trials
  19. Compliance with ICH GCP guidelines in data management
  20. Data management for real-world evidence studies

Protocols Covered across various focussed areas under Cdm Summer Internship

  1. Designing and implementing clinical trial databases
  2. Electronic data capture system setup and management
  3. Data cleaning and validation protocols
  4. Adverse event reporting in clinical trials
  5. Data integrity checks for clinical data management
  6. Designing and managing eCRFs in clinical trials
  7. Data query management systems
  8. Risk-based monitoring implementation in clinical data management
  9. Database locking and freezing procedures
  10. Compliance with CDISC standards in clinical data management

Duration: 5, 10, 15, 20, and 30 Days

Note: Please cross confirm whether internship slots for this field are available before joining.

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Application Process and Other info