Internship Opportunity
Position ID# : Q-IN-F2018-PS092
Jobs Title : Clinical Trial Assistant – Intern (CTA)
No of Openings : 4

Job Classification: Internship (Unpaid)

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

Practicum Learning Shadowing SME

This Training as Internship program provides students hands-on about the various tasks and duties performed by Clinical Research Associate at Pharmaceutical, Hospital and Research Organizations towards conduction of Clinical Trials and project management tasks. This Unpaid Internship is conducted for 11 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 once a week for minimum 3 hours/ day via GoTo Meeting / WebEx sessions. The sessions will educate the Intern on the CRA 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

  • Drug Discovery and Research Process
  • Pre-Clinical Research
  • Introduction to Clinical Trials
  • Role of Clinical Research Associate
  • Phase I Clinical Trials
  • Phase II Clinical Trials
  • Phase III Clinical Trials
  • Phase IV Clinical Trials
  • Good Clinical Practice and ICH Guidelines
  • FDA Regulations
  • Institutional Review Board (IRB)
  • Overview of Clinical Protocol
  • Clinical Protocol Design and Development
  • SOP Development
  • Case Report Form (CRF) Design and Data Capture
  • Clinical Trial Budget
  • Conducting Multinational Clinical Trials
  • Communication with Cross Functional Team
  • Clinical Research Associate In House Responsibilities
  • Selection of Investigator
  • Vendor Selection and Management
  • Informed Consent Preparation
  • Roles and Responsibilities of Investigator
  • Investigator Meetings and Timelines
  • Selection of Investigator Site
  • Study Initiation
  • In-House Monitoring and Reporting
  • Trial Master File (TMF)
  • Introduction to Adverse Events (AE) Reporting and Classification
  • Preparation for Internal Audit
Successful Intern will be provided an opportunity for Interviews to work as consultant for CTA roles at client sites as consultant and as full-time employee with Qtech.
Education :
Biology, Biochemistry, Chemistry, Clinical Research, Medicine, Nursing, Pharmacy, Public health, Pharmacology, or toxicology, Microbiology, Psychology and Sociology.
Experience : 0-2 years
Program Start Date: 10-15-2018 (mm-dd-yy)
Program End Date: 11-28-2018 (mm-dd-yy)
Application Due Date: 10-11-2018 (mm-dd-yy)

Please forward Your resumes along with ID to