Jobs Opening
Position ID :Q-IN-2017-PS036
Date Posted : 03-16-2017 (mm-dd-yyyy)
Jobs Title : Clinical Data Management - Intern
No of Openings : 4

Job Classification: Internship

Qtech Solutions Inc.
3 Executive Drive, Suite 320
Somerset, New Jersey USA 08873.
Director Operations
NJ Phone : 732-770-4100 Fax: 888-532-0210
Email      :

Job Duties

This Training as Internship program provides students hands-on about the various tasks and duties performed by Clinical Research Data Management Professional at Pharmaceutical, Hospital and Research Organizations towards conduction and project management tasks of Clinical Research Data Management for conduction of Clinical Trials. This Unpaid Internship is conducted for 12 Weeks to Fresh and Alumni Students. Selection for Internship is based on GPA and Interview performance. Interns will have the option to participate in person at Somerset, NJ or attend remotely. Students attending the Internship remotely must plan to attend classes thrice a week for minimum 3 hours/ day via GoTo Meeting / WebEx sessions. The sessions will educate the Intern on the CDM task to perform, client settings followed in Industry and will be allocated tasks for submission. During Internship, the candidate will have access to Qtech Proprietary forms, data and related presentations. The Intern will be exposed to various Job related hypothetical tasks to gain experience. The tasks are evaluated to provide feedback to Intern as part of the learning gained. Interns who have successfully completed the Internship, will be provided a certificate of completion. Our Placement division supports various pharmaceutical, healthcare and financial firms, by providing staffing resources meeting cost efficiency, time saved and commitment to their hiring needs. Successful Intern, will be provided an opportunity to work at our client sites on contract as full-time employee of Qtech with benefits.

Learning’s Gained during this Internship / Duties.

  • Introduction to Clinical Trials
  • Phase I Clinical Trials.
  • Phase II Clinical Trials.
  • Phase III Clinical Trials.
  • Phase IV Clinical Trials.
  • Good Clinical Practice And ICH Guidelines
  • SOP Development
  • Communication With Cross Functional Team
  • Introduction to Clinical protocol
  • Foundation of Clinical Data Management
  • Good Clinical Data Management Practices (GCDMP)
  • Data Management Plan
  • Clinical Trial Data and Its Quality
  • Clinical Data Management System
  • Clinical Data Repository
  • Loading the external data into the CDM system
  • Exporting Data to DMC
  • Clinical trial data cleaning and validation
  • Query Management
  • Data Clarification Form
  • Patient Diaries & Patient Reported Outcome
  • Remote Data Entry
  • Clinical Data Entry - I
  • SAE Reconciliation - II
  • Elements of CRF
  • e-CRF Design & Data Tracking
  • Types of Reports Generated
  • Database Locking
  • Clinical Data Archiving
Education : Bioinformatics, Biotechnology, Medical Device & Technology, Biomedical Engineering, Information Technology (IT).
Experience : 0-2 years
Application End Date: 06-16-2017 (mm-dd-yy)

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