New Jersey 732.770.4100

 Clinical Research Data Management

A Clinical Research Data Management specialist coordinates and manages data for clinical research studies. CDM specialist is responsible for clinical study databases and associated data. Being a key member of the interdisciplinary clinical research team CDM works directly and indirectly with Contract Organizations (CROs) for data coordination, validation, and management for compliance with Standard Operating (SOP) procedures, client guidelines, domestic and regulatory agencies.


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Admission Requirements   Recommended: minimum a Bachelor degree in Life Science, Biological Science, Pharmacy, Biochemistry, Health Information Technology
Curriculum Overview 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.
Teaching Methodology Available as self paced training (PIP, pure internet program)
Career Opportunity Pathways Clinical Data Manager
Duration 45 days
Program Brochure 'Click here'   to download program brochure
Contact Information NJ Office - (P) 732.770.4100
Fax - 888.532.0210
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