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CDM Internship

Join NTHRYS for a Clinical Data Management (CDM) Internship to learn about data collection, management, and analysis in clinical trials, focusing on data quality, regulatory compliance, and the use of CDM software.

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CDM Internship

Advanced Focused Areas for Interns in CDM Internships

Internships in 200+ fields

Info @ +91-7993084748
Fee as low as Rs 6000 / 10 Days Duration
Click Here for Application Process
Important Note
Note 1: Candidates may select any one of the focused areas listed below for their internship.
Note 2: Fundamental concepts are provided as guidance for candidates who require them; however, candidates may choose to bypass these sections if desired.
Note 3: All candidates will gain practical, hands-on experience with every step outlined in the provided methodology.
Note 4: Comprehensive placement assistance and career guidance will be available to all candidates during and after the internship.
Note 5: We understand that many students may lack basic practical exposure due to shortcomings in their college education. This is not the fault of the students but rather a failure of the institutions and their staff. At NTHRYS, our staff excel at training every student from the ground up, ensuring they gain the necessary skills and experience.
Back to All Internships CDM Internship Fee Details
  1. Clinical Data Management Process
  2. Data Collection and CRF Design
  3. Electronic Data Capture (EDC) Systems
  4. Data Validation and Cleaning
  5. Database Design and Build
  6. Quality Control and Quality Assurance in CDM
  7. Adverse Event Reporting in CDM
  8. Data Lock and Unlock Procedures
  9. Regulatory Compliance in CDM
  10. CDM Tools and Software
  11. Coding and Terminologies in CDM
  12. Data Integration in CDM
  13. Data Standardization and CTMS
  14. Handling Missing Data in CDM
  15. Clinical Trial Data Privacy and Security
  16. Data Management Plan (DMP)
  17. Metadata Management in CDM
  18. Site Management and Monitoring in CDM
  19. Audit Trails and Traceability in CDM
  20. Role of CDM in Clinical Trials
  21. Biostatistics and CDM Integration
  22. Data Review and Discrepancy Management
  23. Risk-Based Monitoring in CDM
  24. Electronic Health Records (EHR) Integration with CDM
  25. Regulatory Submission Preparation in CDM
  26. Vendor Management in CDM
  27. Role of CDM in Post-Marketing Surveillance
  28. Patient-Reported Outcomes and CDM
  29. Global Trials and Multilingual Data Management in CDM
  30. Future Trends in Clinical Data Management

  1. Clinical Data Management Process Topics

    Analyzes the comprehensive workflow of clinical data management, encompassing data collection, entry, validation, cleaning, and final database lock.

  2. Data Collection and CRF Design Topics

    Discusses the principles and techniques involved in designing Case Report Forms (CRFs) and methodologies for data collection in clinical trials.

  3. Electronic Data Capture (EDC) Systems Topics

    Evaluates the role and impact of Electronic Data Capture (EDC) systems in modern clinical trials, highlighting their benefits, challenges, and integration capabilities.

  4. Data Validation and Cleaning Topics

    Explores the methodologies for ensuring data integrity in clinical trials through rigorous validation and cleaning processes before analysis.

  5. Database Design and Build Topics

    Focuses on the strategies for effective database design and development tailored to clinical trials, ensuring efficient data storage, retrieval, and management.

  6. Quality Control and Quality Assurance in CDM Topics

    Investigates the practices of quality control (QC) and quality assurance (QA) in clinical data management to uphold data integrity and regulatory compliance.

  7. Adverse Event Reporting in CDM Topics

    Examines the processes for capturing, reporting, and managing adverse events (AEs) and serious adverse events (SAEs) within clinical trials.

  8. Data Lock and Unlock Procedures Topics

    Delivers insight into the protocols for locking and unlocking clinical trial databases, including criteria for data lock and procedural steps for unlocking data.

  9. Regulatory Compliance in CDM Topics

    Reviews the regulatory frameworks governing clinical data management, with a focus on GCP, 21 CFR Part 11, and GDPR requirements.

  10. CDM Tools and Software Topics

    Investigates the tools and software utilized in clinical data management, including database systems, EDC platforms, and data analysis applications.

  11. Coding and Terminologies in CDM Topics

    Analyzes the importance of coding systems and standard terminologies, such as MedDRA and WHO Drug, in clinical data management.

  12. Data Integration in CDM Topics

    Explores the challenges and strategies for integrating data from various sources in clinical trials, ensuring consistency and reliability in the resulting datasets.

  13. Data Standardization and CTMS Topics

    Highlights the role of data standardization and the use of Clinical Trial Management Systems (CTMS) in maintaining data uniformity and quality across trials.

  14. Handling Missing Data in CDM Topics

    Discusses the methodologies for addressing missing data in clinical trials, including imputation techniques and their implications on trial outcomes.

  15. Clinical Trial Data Privacy and Security Topics

    Examines the importance of maintaining data privacy and security in clinical trials, focusing on data protection measures and adherence to global privacy regulations.

  16. Data Management Plan (DMP) Topics

    Reviews the critical components of a Data Management Plan (DMP) in clinical trials, outlining its role in guiding data management activities and ensuring compliance.

  17. Metadata Management in CDM Topics

    Explores the management of metadata in clinical trials, discussing its importance in data documentation, retrieval, and long-term usability.

  18. Site Management and Monitoring in CDM Topics

    Discusses the role of site management and monitoring within clinical data management, ensuring data quality and compliance across trial sites.

  19. Audit Trails and Traceability in CDM Topics

    Focuses on the significance of maintaining audit trails and traceability in clinical trials, ensuring transparency and data integrity throughout the study lifecycle.

  20. Role of CDM in Clinical Trials Topics

    Analyzes the pivotal role of clinical data management in clinical trials, emphasizing its impact on data quality, trial timelines, and regulatory submissions.

  21. Biostatistics and CDM Integration Topics

    Explores the integration of biostatistics with clinical data management, highlighting the collaboration between data managers and biostatisticians for accurate analysis.

  22. Data Review and Discrepancy Management Topics

    Discusses the methodologies for reviewing clinical trial data and managing discrepancies, ensuring data consistency and resolving data issues effectively.

  23. Risk-Based Monitoring in CDM Topics

    Focuses on the application of risk-based monitoring in clinical data management, identifying high-risk data points and implementing targeted monitoring strategies.

  24. Electronic Health Records (EHR) Integration with CDM Topics

    Examines the integration of Electronic Health Records (EHR) with clinical data management systems, discussing the benefits and challenges of EHR data in clinical trials.

  25. Regulatory Submission Preparation in CDM Topics

    Reviews the processes involved in preparing clinical trial data for regulatory submissions, including data compilation, dataset preparation, and compliance with regulatory standards.

  26. Vendor Management in CDM Topics

    Discusses the management of third-party vendors in clinical data management, focusing on vendor selection, oversight, and collaboration for data services.

  27. Role of CDM in Post-Marketing Surveillance Topics

    Analyzes the role of clinical data management in post-marketing surveillance, emphasizing the collection and analysis of safety data and real-world evidence.

  28. Patient-Reported Outcomes and CDM Topics

    Explores the integration of patient-reported outcomes (PROs) within clinical data management, highlighting their collection, validation, and analysis in trials.

  29. Global Trials and Multilingual Data Management in CDM Topics

    Discusses the challenges and solutions for managing data in global clinical trials, including multilingual data collection and cross-cultural standardization.

Other Categories

Contact Via WhatsApp on +91-7993084748 for Fee Details

Note: Interns get complete handson exposure to all steps in the allocated methodology.
Fee, Application Process and Other Details: Please visit NTHRYS Internship Program Fees

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