Student Training | Clinical Data Lessons | CDM
Course:  CDM Projects – Role based Tasks
Code:  CDPM
Delivery:
Virtual – Job Focused Self-Paced Online.
(Along Exercise Solutions – Role based tasks)
Post Training Assistance (PTA):
Includes resume support, narrative and mock.
Duration:  4 Weeks / 100 Hours
Online Access :
Qtech-Learning Management System (Q-LMS)
Fees : $1009.00 USD
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Course Description:

Qtech-Sol is a Clinical Science Training Provider. This course provides role-based project exercises with hypothetical documents to conduct clinical trials as CDM Manager or Specialist. This is a job and title focused program. The course emphasizes about role of CDM towards clinical data capture, validating, auditing, and reporting tasks. The course curriculum is designed to give an edge to obtain job as CDM with Pharmaceuticals, Biotech, Medical Device, Clinical Research Organizations (CROs) and with Research Clinics.

The Clinical Research Data Manager will develop and manage core area of clinical data obtained thru clinical trials or post marketing surveillance. The student will be shared with following project scenarios to perform following tasks : Introduction to Clinical Trials, Protocol Design and Development, Data Management Plan, Data Cleaning and Data Validation, Query Management, Coding of Adverse Events, SAE Reconciliation, Elements of CRF, e-CRF designing Data tracking off CRFs.

  • Admission Requirements:

    Recommended: An Associate or bachelor’s degree in Statistics, Biostatistics, Biotechnology, Economics, Computer Science, Engineering, Cognitive Science, Data Science, Machine Learning (ML), Artificial Intelligence (AI), Mathematics.

  • Learning Outcomes:
    The Benefit Student Gains

    The Benefit Student Gains

    • Upgrading the Knowledge required.
    • Better Resume Placement for promising jobs.
    • Low Investment, high learnings
    • Learn from Anywhere, Anytime at your pace.
    • Job and Title Based Tasks as followed and Practiced in industry
    • Applying Concept into Real-time (Policies, governance and tools)
    • Work on Role Based Tasks followed and Practiced in industry
    • Mocks and Narratives for Client Discussions
    • Readiness to work with limited support
  • Career Pathways

    The program objective is to help Clinical Data Management to meet the following career pathways, after completing this practicum program. Students can apply for below open job titles based on highest education background and prior experiences (if any).

CLINICAL DATA MANAGEMENT JOB TITLES
  • Clinical Data Manager
  • Clinical Research Data Analyst
  • Clinical Data Associate
  • Case Report Form Designer
  • Data Quality Manager
  • Clinical Business Analyst

The Clinical Research Data Management training program offered at Qtech provides insights into Clinical Research Data Management activities along with exposure to real-time documentation and scenarios pertaining to roles and responsibilities performed by Clinical Data Management specialist. Qtech provides in-depth into the core area of clinical data management like Clinical data and its quality, data management plan, data entry, Clinical Research Data Management Systems (CDMS), Clinical data repository, loading of external data into CDM, Query management, data clarification form, database locking, patient diary, data cleaning and validation, and database archiving. The students will get practical exposure to real-time documentation and scenarios for Data Management Plan, Query Management, Coding of Adverse Events, SAE Reconciliation, Data Cleaning and Data Validation, Elements of CRF, e-CRF designing, Data tracking from CRF, and Types of Reports generated.

Clinical Data Management – Role based Projects (CDMP)
LIST OF TOPICS:

THEORETICAL ASPECT OF THE FIELD:

1. Introduction to Clinical Trials

2. Protocol Design and Development

3. Protocol

4. Data Management Plan

5. Query Management

6. SAE Reconciliation

7. Introduction to Adverse Event Reporting and Classification

8. AE Coding

9. Clinical Trial Data Cleaning and Validation

10. Elements of CRF

11. E CRF Design and Data Tracking

12. Trial Master File (TMF)

13. CTMS Track Recording

14. Database Lock

  • The program gave me an in-depth understanding of the role of a CDM in Clinical Research and Trial Management Teams. With the practical examples and lectures from professionals, I gained a clear understanding of the practical applications needed for work. Very good course work!

    Vinuthna D (Chicago, IL)Ramya I (New Jersey)

  • The best part about CDM training is presentations which clearly mention the important and key points that are helpful for building basics in the subject. I found the exercises helpful in understanding the format on how to fill the forms and analyzing the data which will be useful in real-time for me.

    Elizabeth U (New Jersey)

  • I am a Biomedical Science graduate. This Certificate training helped me to understand the Job-related work process better. The Clinical Data Management training program offered at Qtech is very useful for beginners, I liked it and highly recommend others. Currently, I am enrolled in an Internship program to meet my career goals.

    Pratibha T. (Seattle, WA)

  • Category:
    Data Management
  • Duration:
    04 Weeks / 100 Hours
  • Price:
  • Language:
    English