OUR TRAINING PROGRAMS

     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. Alternatively, if you prefer the traditional classroom approach, our Blended Classroom Program (BCP).

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 3 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
  • Blended Classroom Program (BCP)
    • – 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)
  • University Alliance Programs (UAP)
    • - Colleges/Universities (Student Internships/Career Enhancement)
  • State Funding Programs (SFP)
    • - State Funded Programs (For Unemployed and Career Changers)
  • High School Programs (HSP)
    • - Applies for Grade 12 - Health Science / High School Students

 

Choose your education level from the links below, and see which programs are available for you!

MASTERS / BACHELORS

Clinical Research Associate

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 Clinical 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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Clinical Research Project Management (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 Associate

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 (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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Drug Safety Data Management (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 Data Management

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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Healthcare Business Analyst - Basics

A Healthcare Business Analyst is a professional employed by a Healthcare and pharmaceutical organization, who keep track of the reforms ,

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Managed Care Business Analyst

The purpose of analytics in a healthcare organization is to create insights that help achieve strategic goals such as improving clinical quality,

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Clinical Data Oriented Training

The Clinical Data Oriented Training (CDOT) 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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SAS Basics -Base, Macros, Sql

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, Graphs

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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Associate / Undergraduate

Clinical Research Coordinator

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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Clinical Trial Assistant

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. Advanced CRA training is designed for experienced professionals.

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Pharmacovigilance Assistant

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 , GCP and Clinical Safety guidelines per U.S. and international markets.

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High School (Grade 12)

Clinical Trial Assistant (CTA)

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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Clinical Data Assistant (CDA)

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

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Healthcare Business Associate

A Clinical Research Project / Study Manager (CRM) is responsible for the monitoring, data collection and analysis, and reporting of clinical trials.

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Contact

Qtech Solutions Inc

3 Executive Drive
Suite 320, Somerset
New Jersey 08873 USA

Phone: 732-770-4100, 732.563.2233
Fax: 888-532-0210
Mail: info@qtech-solutions.com