A Clinical Data Management specialist coordinates and manages data for clinical research studies. CDM specialist is responsible for clinical study databases and associated data.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.
Our Programs are delivered in 2 Different ways for convenience of student:
• Self-Paced Individual Program (SIP)
– Skill and Job Oriented Certificate programs, delivered as Self-Paced Online with project solutions.
• Self-Paced Blended Program (SBP)
– Skill and Job Oriented Certificate programs, delivered as Self-Paced Online with project solutions. Support thru Email and Phone for queries. Student participates in 7 days Post Training Assistance program for Resume preperation.
|Category: Clinical Data Management||Lessons: 28 Lessons||Duration: 06 Weeks / 175 Hours||Language: English|
Clinical Research Data Management program is Approved by New Jersey Department of Education and Department of Labor and Workforce, United States.
Recommended: An Associate or bachelor’s degree in medicine, Nursing, Pharmacy, Public health Biology, Biochemistry, Biomedical engineering, Biotechnology, Chemistry, Clinical Research, Public health, Pharmacology, or toxicology, Medical Device & Technology, Psychology, Sociology and Healthcare Administration.
Institutional Scholarship / Promotion is available for selected on tuition. We review your education background, certifications, and prior experiences (if applicable), to evaluate your eligibility. Qualified student will be provided with the promo code for scholarship on Tuition.
Please Email your resume to Human Resources email@example.com to check on your eligibility. We will contact you. Qtech's objective is to provide you the right career pathway and advancement required to meet your career goals.
The Benefit Student Gains
Our objective is to help students to meet the following career pathways. Typical Clinical Research Data Management (CDM) Job Titles the candidates can apply after this training program are :
|CLINICAL DATA MANAGEMENT JOB TITLES|
|Clinical Data Manager||Documentation Specialist|
|Principal Clinical Data Manager||Data Analyst / SAS Programmer (CDM)|
|Senior Clinical Data Manager||Clinical Data Analyst|
|CRF Designer||Clinical Business Analyst|
|QA / QC Analyst||Clinical Data Audit Manager|
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 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 RESEARCH DATA MANAGEMENT
LIST OF TOPICS:
THEORETICAL ASPECT OF THE FIELD:
1. Introduction to Clinical Trials
2. Phase I Clinical Trials.
3. Phase II Clinical Trials.
4. Phase III Clinical Trials.
5. Phase IV Clinical Trials.
6. Good Clinical Practice And ICH Guidelines
7. SOP Development
8. Communication With Cross Functional Team
9. Introduction to Clinical protocol
10. Foundation of Clinical Data Management
11. Good Clinical Data Management Practices (GCDMP)
12. Data Management Plan
13. Clinical Trial Data and Its Quality
14. Clinical Data Management System
15. Clinical Data Repository
16. Loading the external data into the CDM system
17. Exporting Data to DMC
18. Clinical trial data cleaning and validation
19. Query Management
20. Data Clarification Form
21. Patient Diaries & Patient Reported Outcome
22. Remote Data Entry
23. Clinical Data Entry - I, SAE Reconciliation - II
24. Elements of CRF
25. e-CRF Design & Data Tracking
26. Types of Reports Generated
27. Database Locking
28. Clinical Data Archiving
LIST OF EXERCISES:
CASE 1. Introduction to Clinical Trials
CASE 2. Protocol Design and Development
CASE 3. Data Management Plan
CASE 4. Data Cleaning and Data Validation.
CASE 5. Query Management.
CASE 6. Coding of Adverse Events.
CASE 7. SAE Reconciliation.
CASE 8. Elements of CRF.
CASE 9. e-CRF designing Data tracking from CRF
5.00 average based on 3 ratings
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 about the practical applications needed for work. Very good course work!
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.
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 into Internship program to meet my career goals.