Clinical Research Data Management program is Approved by New Jersey Department of Education and Department of Labor and Workforce, United States.
Recommended: Minimum a Bachelor or Master degree in Medicine, Nursing (RN), Pharm D, Public Health, Pharmaceutical and Industrial Chemistry.
Available as self paced training (PIP, pure internet program) Course Reading Material (chapters, PowerPoint presentations, Exercises, Quizzes & Final Exam).
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.
1) Upgrading the Knowledge required.
2) Better Resume Placement for promising jobs.
3) Low Investment, high learnings
4) Learn from Anywhere, Anytime at your pace.
5) Title Based learning.
Institutional Scholarship is available for selected on tuition. We review your education, certifications, and experiences (if applicable) to evaluate the eligibility and if found qualified an Institutional scholarship will be awarded on Tuition. Email us your resume to email@example.com to check on your eligibility. We will email you the details of the program along with eligible scholarship. Qtech’s objective is to provide you the right career pathway and advancement required to meet your goals.
The Post Training Assistance (PTA) program is provided to candidates who have completed Qtech-Sol Certification training program.
Program is designed by industry experts for fresh graduates and professionals. The training provides in depth knowledge of roles and responsibilities of Clinical Research Data Management.View details
Proceed to REGISTER for demo Access. Upon Login using your user-id and password, you will have access to first lesson for next 5 days.
The program gave me an in-depth understanding of the role of a DSA in Clinical Research and Pharmacovigilance department. 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 DSA 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 Medical Science graduate. This Certificate training helped me to understand the Job related work process better. The Drug Safety Associate 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.
3 Executive Drive
Suite 320, Somerset
New Jersey 08873 USA