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CLINICAL SCIENCE PRACTICUM TRAINING And Certification

CLICK FOR THE PROGRAM YOU ARE ELIGIBLE.


     APPROVED BY





Qtech - Sol Professional Development Center (QPDC) is a Private Vocational School (PVS) approved by New Jersey Department of Education and Department of Labor and Workforce Development.

  

At Qtech Solutions Inc, our training programs are designed to help you move forward in your chosen career, by helping you learn these vital roles that are in demand with pharmaceutical and healthcare companies across the US. We know that you have a busy life, so each program is designed to help pace yourself on your own time, allowing you to advance your career without the fiscal and physical strain of a traditional classroom setting. Our Pure Internet Program (PIP) or Blended Online Program (BIP) can be managed on your laptop or tablet, allowing you to fit in lessons whenever you have the time.

Our courses are approved by the State of New Jersey Department of Education and Department of Labor and Workforce and are the equivalent of 2 years of practical work experience. Browse through our catalog below and choose the course that's right for you!.

             PROGRAM DELIVERY SYSTEMS

Our Programs are Available in 2 Different Delivery Systems:

  • Pure Internet Program (PIP)
    • - A Self-Paced Online Program with Email     Support Provided
  • Blended Internet Program (BIP)
    • - A Self-Paced Online Program with Email     Support Provided



FIND THE RIGHT MODEL FOR YOUR EDUCATIONAL LEVEL

When beginning one of our training programs, it's important for you to choose the programs that match your current education and skill level. We offer a wide range of programs designed to engage any age or education level and help see how you're best suited to.

Our programs include:

  • Career Advancement Programs (CAP)
    • - Applies for Individuals and Working Professionals    (Masters/Bachelors)
  • Client Setting Programs (CSP)
    • - Applies for Entry Level/Beginners    (Associate/Undergraduates)

Gain the Experience
You Need to Get Started


Overcome the hurdles in getting your first job with our training practicums. Designed like an internship, you can shadow our experts to learn more about the positions you will be moving into and gain valuable networking connections. We are ready to help build the foundation for the rest of your career.



Clinical Research Programs

Clinical Research Associate / Coordinator (CRAT)

A Clinical Research Associate / Coordinator in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support progress of clinical trials.

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Advanced Clincial Research Associate (ACRA)

A Clinical Research Associate in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support progress of clinical trials.

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Additional Advanced Clinical Research (AACR)

A Clinical Research Project / Study Manager (CRM) is responsible for the monitoring, data collection and analysis, and reporting of clinical trials performed and be in compliance with Ethical practices, ICH,

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Drug Safety-Pharmacovigilance Programs

Drug Safety-Pharmacovigilance Associate (DSAT)

A Drug Safety / Pharmacovigilance Associate (DSA / PVA), known also in the industry as a Pharmacovigilance Officer, is a health science professional responsible for the monitoring, data collection and analysis,

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Advanced Drug Safety Associate (ADSA)

A Drug Safety Associate (DSA) is responsible for the monitoring, data collection and analysis, and reporting of drug safety information for compliance with drug safety regulations in the U.S. and international markets.

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Additional Advanced Drug Safety (AADS)

A Drug Safety Data Management roles towards project Management and report submissions (DSA) is responsible for the monitoring, data collection and analysis, and reporting of drug safety information for compliance with drug safety


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CLINICAL SCIENCE PACKAGE PROGRAMS

Drug Safety-Pharmacovigilance Data Management (DSPM)

A Drug Safety-Pharmacovigilance Data and Safety Monitoring and report submissions to Authorities.Responsible for the monitoring,data collection and analysis,and reporting of drug safety information for compliance with drug safety regulations per international markets.

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Clinical Research Project Management and Trial Monitoring (CRPM)

A Clinical Research Project / Study Manager(CRM) is responsible for the monitoring, data collection and analysis, and reporting of clinical trials performed and follow Ethical practices, ICH, GCP, and Clinical Safety guidelines per international markets.

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Clinical Data Management Programs

Clinical Research Data Management (CDMT)

A Clinical Data Management specialist coordinates and manages data for clinical research studies. CDM specialist is responsible for clinical study databases and associated data.

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Clinical Trial Data Analysis and Reporting (CDAR)

The Clinical Trial Data Analysis and Reporting (CDAR) provides intensive learning on how SAS is used in clinical and pharmaceutical industries. In particular, how codes, analysis and reports are generated using SAS.

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Clinical - Assistant Programs

Clinical Trial Assistant (CTAA)

A Clinical Research Assistant is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support administrative support, assisting with routine tests and procedures and collecting both data and samples.

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Pharmacovigilance Assistant (PVAA)

The process of drug development is generally divided into two stages: (1) new lead discovery (preclinical research), and (2) new product development (clinical development). Drug Safety - Pharmacovigilance Assistant can work in Pharmaceuticals, Medical Device, Hospitals,

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SAS SOFTWARE Programs

SAS Basics - Base SAS, Macros, Sql Modules (BSAS)

SAS program is the industry-standard statistical tool. QPDC offers Basic SAS Modules training program, which is designed to help interested candidates understand how SAS program manipulates and views data in various industries.

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SAS Advanced - Stat and Graph Modules (SSAS)

SAS program is the industry-standard statistical tool. QPDC offers Advanced SAS Modules training program, which is designed to help interested candidates understand how SAS program manipulates and views data in various

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Contact

Qtech Solutions Inc

2250 Boundary Road, Unit # 208
Burnaby, BC - V5M 3Z3
CANADA

Phone: 604.757.7733
Mail: qpdc@qtech-solutions.ca