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.
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!.
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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.
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.
CRA (in House) supports in-house monitoring and clinical trials progress to ensure the integrity of the trial scientific data collected and the clinical protocol.
| Admission Requirements | Recommended: minimum a Bachelor degree in biochemistry, biomedical engineering, biotechnology, chemistry, clinical data management, medicine, pharmaceutical engineering, industrial pharmacy, industrial chemistry, public health, pharmacy, pharmaceutical business, pharmacology, or toxicology. |
| Curriculum Overview | The course provides a thorough foundation in clinical trial science, the drug development process, and clinical trial design methodology. It includes a protocol development, assessment and reporting of adverse events and explains GCP-ICH guidelines along with other necessary regulatory information. The course emphasizes on understanding of the science and the expectations of initiating, conducting, monitoring, and managing clinical trial related work. This training will develop the technical skills and knowledge pertaining to roles and responsibilities of CRA - In House. Students will get exposure to real time practices pertaining to Case Report forms (CRFs), Trial Master File (TMF), Clinical Trial Protocol, Clinical Trial Budget and Audit. The course curriculum was designed to give an edge to obtain job opportunity in clinical research field. |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) Course Reading Material (chapters, PowerPoint presentations, Exercises, Quizzes & Final Exam) |
| Certificate of Completion |
Pass grade requires minimum 75% score on the final exam. |
| Career Opportunity Pathways | Clinical Research Associate / Coordinator, Clinical Research Monitor, Trial Documentation Specialist, CRA - Trial master File Maintenance, CRA - Trial Documents Validation and CRF Data |
| Duration | 45 days |
| Demo | 'Click here' to access course demo |
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.
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.
CRA ensures the integrity of the trial scientific data collected and the clinical protocol.Advanced CRA training is designed for experienced professionals to add new skills set. See program highlights for more information
| Admission Requirements | Recommended: minimum a Bachelor degree in biochemistry, biomedical engineering, biotechnology, chemistry, clinical data management, medicine, pharmaceutical engineering, industrial pharmacy, industrial chemistry, public health, pharmacy, pharmaceutical business, pharmacology, or toxicology. |
| Curriculum Overview | The course is designed for experienced professionals to add new skills set and therefore prior
training or relevant experience is required. The ACRA covers 15 advanced topics and 15 advanced
exercises and provides exposure to diverse CRA responsibilities, real time documentation + advanced
learning supported by practical case scenario tasks and follow up process. Specifically, the topics
ACRA training covers includes:
|
| Teaching Methodology | Available as self paced training (PIP, pure internet program) Course Reading Material (PowerPoint presentations and Exercises). |
| Career Opportunity Pathways | Clinical Research Associate (In-House), Clinical Research Monitor, Trial Documentation Specialist, CRA - Trial master File Maintenance, CRA - Trial Documents Validation and CRF Data. |
| Duration | 45 days |
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,
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.
The Additional CRA training emphasizes on practical aspects as presentations in the reference to role performed by CRM into industry. See program highlights for more information.
| Admission Requirements | Recommended: Minimum a Bachelor degree in biochemistry, biomedical engineering, biotechnology, chemistry, clinical data management, medicine, pharmaceutical engineering, industrial pharmacy, industrial chemistry, public health, pharmacy, pharmaceutical business, pharmacology, or toxicology. |
| Curriculum Overview | Our program is approachable which provides in-depth knowledge and practical exposure to roles and responsibilities performed by Clinical Research Project Manager / Study Manager. It gives insight into topics including but not limited to: LIST OF TOPICS :
|
| Teaching Methodology | Available as self-paced training (PIP, pure internet program) Course Reading Material (PowerPoint presentations with Voice-over). |
| Career Opportunity Pathways | Clinical Program Manager, Senior Clinical Research Associate, Clinical Study Manager, Research Business Manager. |
| Duration | 45 days |
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,
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, and reporting of drug safety information for compliance with drug safety regulations in the U.S. and international markets.
DSA / PVA also monitors and assesses drug safety requirements for drugs in the development pipeline as well as for those drugs approved that may require additional marketing or clinical action by the drug manufacturer. See program highlights for more information.
| Admission Requirements | Recommended: minimum a Bachelor degree in Public Health/Medicine, Pharmaceutical Chemistry, Pharmacy, Medical Technology, Pharmacy,Nursing, Pharmacology,Toxicology, Industrial Pharmacy, Healthcare professionals (RN, PA, MD, PT.PRh, PharmD or Medical Technologist) |
| Curriculum Overview | Our program is approachable which provides in-depth knowledge and practical
exposure to roles and responsibilities performed by Drug Safety / Pharmacovigilance Associate.
It gives insight into base topics including but not limited to: Introduction
to Clinical Research, Drug Development Process, ICH Guidelines for Good Clinical
Practice, Drug Safety Regulations and Guidelines, Clinical Trial Protocol, SOP
Development, Drug Safety Databases and Software, and Understanding of 21 CFR Part
11 and HIPAA. Our program focuses on core topics of Drug Safety in reference to roles and responsibilities performed by Drug Safety / Pharmacovigilance Associate. Core topics includes Role of DSA (Trials), Clinical Trial Safety Surveillance, Phase IV Trials and Pharmacovigilance, Introduction To Adverse Events, SAE Reconciliation, Characteristics of a Case, Sources of Individual Case Reports, Basics of Coding in Drug Safety, Case Narratives, Case Follow-up Approaches and Handling of Cases and Drug Safety Data Extraction and Pre-processing. Thus, Program offered at Qtech will provide students an edge to get into opportunities in the Drug Safety field. |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) |
| Career Opportunity Pathways | Drug Safety / Pharmacovigilance Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety / Pharmacovigilance Associate, Medical Reviewer |
| Duration | 45 days |
| Demo | 'Click here' to access course demo |
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.
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.
The Advanced DSA training emphasizes on practical aspects in the reference to role performed by DSA into industry. See program highlights for more information.
| Admission Requirements | Recommended: minimum a Bachelor degree in Pharmaceutical Chemistry, Public Health, Medicine, Pharmaceutical Management, Clinical Research, Pharmacy, Nursing, Pharmacology, Toxicology, Industrial Pharmacy or Industrial Chemistry. Completed DSA training or work experience. |
| Curriculum Overview | The course is designed for experienced professionals to add new skills set and therefore prior training or relevant experience is required. The Advanced DSA provides hands on experience to diverse advanced tasks performed by DSA into Industry. During the program students will:
In particular: |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) Course Reading Material (PowerPoint presentations and Exercises). |
| Career Opportunity Pathways | Drug Safety Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety Associate, Medical Reviewer. |
| Duration | 45 days |
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.
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 regulations in the U.S. and international markets.
The Additional DSA training emphasizes on practical aspects as presentations in the reference to role performed by DSA into industry. See program highlights for more information.
| Admission Requirements | Recommended: Minimum a Bachelor degree in Medicine (MD), Pharmaceutical Chemistry, Pharmacy (PharmD), Nursing (RN). |
| Curriculum Overview | Our program is approachable which provides in-depth knowledge and practical exposure to roles and responsibilities performed by Drug Safety / Pharmacovigilance Data Manager. It gives insight into base topics including but not limited to: LIST OF TOPICS:
|
| Teaching Methodology | Available as self-paced training (PIP, pure internet program) Course Reading Material (PowerPoint presentations with Voice-over). |
| Career Opportunity Pathways | Drug Safety Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety Associate, Medical Reviewer. |
| Duration | 45 days |
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.
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, and reporting of drug safety information for compliance with drug safety regulations in the U.S. and international markets.
DSA / PVA also monitors and assesses drug safety requirements for drugs in the development pipeline as well as for those drugs approved that may require additional marketing or clinical action by the drug manufacturer. See program highlights for more information.
| Admission Requirements | Recommended: minimum a Bachelor degree in Public Health/Medicine, Pharmaceutical Chemistry, Pharmacy, Medical Technology, Pharmacy,Nursing, Pharmacology,Toxicology, Industrial Pharmacy, Healthcare professionals (RN, PA, MD, PT.PRh, PharmD or Medical Technologist) |
| Curriculum Overview | Our program is approachable which provides in-depth knowledge and practical
exposure to roles and responsibilities performed by Drug Safety / Pharmacovigilance Associate.
It gives insight into base topics including but not limited to: Introduction
to Clinical Research, Drug Development Process, ICH Guidelines for Good Clinical
Practice, Drug Safety Regulations and Guidelines, Clinical Trial Protocol, SOP
Development, Drug Safety Databases and Software, and Understanding of 21 CFR Part
11 and HIPAA. Our program focuses on core topics of Drug Safety in reference to roles and responsibilities performed by Drug Safety / Pharmacovigilance Associate. Core topics includes Role of DSA (Trials), Clinical Trial Safety Surveillance, Phase IV Trials and Pharmacovigilance, Introduction To Adverse Events, SAE Reconciliation, Characteristics of a Case, Sources of Individual Case Reports, Basics of Coding in Drug Safety, Case Narratives, Case Follow-up Approaches and Handling of Cases and Drug Safety Data Extraction and Pre-processing. Thus, Program offered at Qtech will provide students an edge to get into opportunities in the Drug Safety field. |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) |
| Career Opportunity Pathways | Drug Safety / Pharmacovigilance Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety / Pharmacovigilance Associate, Medical Reviewer |
| Duration | 45 days |
| Demo | 'Click here' to access course demo |
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.
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.
The Advanced DSA training emphasizes on practical aspects in the reference to role performed by DSA into industry. See program highlights for more information.
| Admission Requirements | Recommended: minimum a Bachelor degree in Pharmaceutical Chemistry, Public Health, Medicine, Pharmaceutical Management, Clinical Research, Pharmacy, Nursing, Pharmacology, Toxicology, Industrial Pharmacy or Industrial Chemistry. Completed DSA training or work experience. |
| Curriculum Overview | The course is designed for experienced professionals to add new skills set and therefore prior training or relevant experience is required. The Advanced DSA provides hands on experience to diverse advanced tasks performed by DSA into Industry. During the program students will:
In particular: |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) Course Reading Material (PowerPoint presentations and Exercises). |
| Career Opportunity Pathways | Drug Safety Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety Associate, Medical Reviewer. |
| Duration | 45 days |
A Clinical Data Management specialist coordinates and manages data for clinical research studies. CDM specialist is responsible for clinical study databases and associated data.
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, and reporting of drug safety information for compliance with drug safety regulations in the U.S. and international markets.
DSA / PVA also monitors and assesses drug safety requirements for drugs in the development pipeline as well as for those drugs approved that may require additional marketing or clinical action by the drug manufacturer. See program highlights for more information.
| Admission Requirements | Recommended: minimum a Bachelor degree in Public Health/Medicine, Pharmaceutical Chemistry, Pharmacy, Medical Technology, Pharmacy,Nursing, Pharmacology,Toxicology, Industrial Pharmacy, Healthcare professionals (RN, PA, MD, PT.PRh, PharmD or Medical Technologist) |
| Curriculum Overview | Our program is approachable which provides in-depth knowledge and practical
exposure to roles and responsibilities performed by Drug Safety / Pharmacovigilance Associate.
It gives insight into base topics including but not limited to: Introduction
to Clinical Research, Drug Development Process, ICH Guidelines for Good Clinical
Practice, Drug Safety Regulations and Guidelines, Clinical Trial Protocol, SOP
Development, Drug Safety Databases and Software, and Understanding of 21 CFR Part
11 and HIPAA. Our program focuses on core topics of Drug Safety in reference to roles and responsibilities performed by Drug Safety / Pharmacovigilance Associate. Core topics includes Role of DSA (Trials), Clinical Trial Safety Surveillance, Phase IV Trials and Pharmacovigilance, Introduction To Adverse Events, SAE Reconciliation, Characteristics of a Case, Sources of Individual Case Reports, Basics of Coding in Drug Safety, Case Narratives, Case Follow-up Approaches and Handling of Cases and Drug Safety Data Extraction and Pre-processing. Thus, Program offered at Qtech will provide students an edge to get into opportunities in the Drug Safety field. |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) |
| Career Opportunity Pathways | Drug Safety / Pharmacovigilance Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety / Pharmacovigilance Associate, Medical Reviewer |
| Duration | 45 days |
| Demo | 'Click here' to access course demo |
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.
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.
The Advanced DSA training emphasizes on practical aspects in the reference to role performed by DSA into industry. See program highlights for more information.
| Admission Requirements | Recommended: minimum a Bachelor degree in Pharmaceutical Chemistry, Public Health, Medicine, Pharmaceutical Management, Clinical Research, Pharmacy, Nursing, Pharmacology, Toxicology, Industrial Pharmacy or Industrial Chemistry. Completed DSA training or work experience. |
| Curriculum Overview | The course is designed for experienced professionals to add new skills set and therefore prior training or relevant experience is required. The Advanced DSA provides hands on experience to diverse advanced tasks performed by DSA into Industry. During the program students will:
In particular: |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) Course Reading Material (PowerPoint presentations and Exercises). |
| Career Opportunity Pathways | Drug Safety Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety Associate, Medical Reviewer. |
| Duration | 45 days |
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.
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, and reporting of drug safety information for compliance with drug safety regulations in the U.S. and international markets.
DSA / PVA also monitors and assesses drug safety requirements for drugs in the development pipeline as well as for those drugs approved that may require additional marketing or clinical action by the drug manufacturer. See program highlights for more information.
| Admission Requirements | Recommended: minimum a Bachelor degree in Public Health/Medicine, Pharmaceutical Chemistry, Pharmacy, Medical Technology, Pharmacy,Nursing, Pharmacology,Toxicology, Industrial Pharmacy, Healthcare professionals (RN, PA, MD, PT.PRh, PharmD or Medical Technologist) |
| Curriculum Overview | Our program is approachable which provides in-depth knowledge and practical
exposure to roles and responsibilities performed by Drug Safety / Pharmacovigilance Associate.
It gives insight into base topics including but not limited to: Introduction
to Clinical Research, Drug Development Process, ICH Guidelines for Good Clinical
Practice, Drug Safety Regulations and Guidelines, Clinical Trial Protocol, SOP
Development, Drug Safety Databases and Software, and Understanding of 21 CFR Part
11 and HIPAA. Our program focuses on core topics of Drug Safety in reference to roles and responsibilities performed by Drug Safety / Pharmacovigilance Associate. Core topics includes Role of DSA (Trials), Clinical Trial Safety Surveillance, Phase IV Trials and Pharmacovigilance, Introduction To Adverse Events, SAE Reconciliation, Characteristics of a Case, Sources of Individual Case Reports, Basics of Coding in Drug Safety, Case Narratives, Case Follow-up Approaches and Handling of Cases and Drug Safety Data Extraction and Pre-processing. Thus, Program offered at Qtech will provide students an edge to get into opportunities in the Drug Safety field. |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) |
| Career Opportunity Pathways | Drug Safety / Pharmacovigilance Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety / Pharmacovigilance Associate, Medical Reviewer |
| Duration | 45 days |
| Demo | 'Click here' to access course demo |
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,
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.
The Advanced DSA training emphasizes on practical aspects in the reference to role performed by DSA into industry. See program highlights for more information.
| Admission Requirements | Recommended: minimum a Bachelor degree in Pharmaceutical Chemistry, Public Health, Medicine, Pharmaceutical Management, Clinical Research, Pharmacy, Nursing, Pharmacology, Toxicology, Industrial Pharmacy or Industrial Chemistry. Completed DSA training or work experience. |
| Curriculum Overview | The course is designed for experienced professionals to add new skills set and therefore prior training or relevant experience is required. The Advanced DSA provides hands on experience to diverse advanced tasks performed by DSA into Industry. During the program students will:
In particular: |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) Course Reading Material (PowerPoint presentations and Exercises). |
| Career Opportunity Pathways | Drug Safety Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety Associate, Medical Reviewer. |
| Duration | 45 days |
A Healthcare Business Analyst is a professional employed by a Healthcare and pharmaceutical organization, who keep track of the reforms ,
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, and reporting of drug safety information for compliance with drug safety regulations in the U.S. and international markets.
DSA / PVA also monitors and assesses drug safety requirements for drugs in the development pipeline as well as for those drugs approved that may require additional marketing or clinical action by the drug manufacturer. See program highlights for more information.
| Admission Requirements | Recommended: minimum a Bachelor degree in Public Health/Medicine, Pharmaceutical Chemistry, Pharmacy, Medical Technology, Pharmacy,Nursing, Pharmacology,Toxicology, Industrial Pharmacy, Healthcare professionals (RN, PA, MD, PT.PRh, PharmD or Medical Technologist) |
| Curriculum Overview | Our program is approachable which provides in-depth knowledge and practical
exposure to roles and responsibilities performed by Drug Safety / Pharmacovigilance Associate.
It gives insight into base topics including but not limited to: Introduction
to Clinical Research, Drug Development Process, ICH Guidelines for Good Clinical
Practice, Drug Safety Regulations and Guidelines, Clinical Trial Protocol, SOP
Development, Drug Safety Databases and Software, and Understanding of 21 CFR Part
11 and HIPAA. Our program focuses on core topics of Drug Safety in reference to roles and responsibilities performed by Drug Safety / Pharmacovigilance Associate. Core topics includes Role of DSA (Trials), Clinical Trial Safety Surveillance, Phase IV Trials and Pharmacovigilance, Introduction To Adverse Events, SAE Reconciliation, Characteristics of a Case, Sources of Individual Case Reports, Basics of Coding in Drug Safety, Case Narratives, Case Follow-up Approaches and Handling of Cases and Drug Safety Data Extraction and Pre-processing. Thus, Program offered at Qtech will provide students an edge to get into opportunities in the Drug Safety field. |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) |
| Career Opportunity Pathways | Drug Safety / Pharmacovigilance Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety / Pharmacovigilance Associate, Medical Reviewer |
| Duration | 45 days |
| Demo | 'Click here' to access course demo |
The purpose of analytics in a healthcare organization is to create insights that help achieve strategic goals such as improving clinical quality,
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.
The Advanced DSA training emphasizes on practical aspects in the reference to role performed by DSA into industry. See program highlights for more information.
| Admission Requirements | Recommended: minimum a Bachelor degree in Pharmaceutical Chemistry, Public Health, Medicine, Pharmaceutical Management, Clinical Research, Pharmacy, Nursing, Pharmacology, Toxicology, Industrial Pharmacy or Industrial Chemistry. Completed DSA training or work experience. |
| Curriculum Overview | The course is designed for experienced professionals to add new skills set and therefore prior training or relevant experience is required. The Advanced DSA provides hands on experience to diverse advanced tasks performed by DSA into Industry. During the program students will:
In particular: |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) Course Reading Material (PowerPoint presentations and Exercises). |
| Career Opportunity Pathways | Drug Safety Associate, Drug Safety Scientist Case Processor, Triage Specialist, Narrative Writer, Medical Record Extractor, Senior Drug Safety Associate, Medical Reviewer. |
| Duration | 45 days |
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.
SAS program is the industry-standard statistical tool. QPDC offers SAS Modules training program, which is designed to help interested candidates understand how SAS program manipulates and views data in various industries. This course prepares candidates to gain solid understanding of functionality of all Three modules of SAS software SAS Base, SAS Macros, SAS SQL.
| Admission Requirements | Recommended: minimum a Bachelor degree in Statistics, Bio-statistics, Biotechnology,
Economics, Clinical Research with IT skills, Computer Science, Engineering, or Applied
Mathematics. Access to: SAS Software (Version 9.X or above) and Windows Microsoft Suite. |
| Curriculum Overview | It is designed to provide programming personnel and analysts or interested candidates with the skills necessary to produce simple reports and data sets as well as providing an understanding of how to SAS to present and analyze data. The focus of the course is to consider SAS in the data processing environment and provide a strong background for programmers to tackle advanced SAS programming skills. All Three modules SAS Base, SAS Macros, SAS SQL, are available in our online learning management system. |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) |
| Duration | 45 days |
| Demo | 'Click here' to access course demo |
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
SAS program is the industry-standard statistical tool. QPDC offers SAS Modules training program, which is designed to help interested candidates understand how SAS program manipulates and views data in various industries. This course prepares candidates to gain solid understanding of functionality of all Two modules of SAS software SAS Stat, SAS Graphs.
| Admission Requirements | Recommended: minimum a Bachelor degree in Statistics, Bio-statistics, Biotechnology,
Economics, Clinical Research with IT skills, Computer Science, Engineering, or Applied
Mathematics. Access to: SAS Software (Version 9.X or above) and Windows Microsoft Suite. |
| Curriculum Overview | It is designed to provide programming personnel and analysts or interested candidates with the skills necessary to produce simple reports and data sets as well as providing an understanding of how to SAS to present and analyze data. The focus of the course is to consider SAS in the data processing environment and provide a strong background for programmers to tackle advanced SAS programming skills. All Two modules SAS Stat, SAS Graphs, are available in our online learning management system. |
| Teaching Methodology | Available as self paced training (PIP, pure internet program) |
| Duration | 45 days |
| Demo | 'Click here' to access course demo |
The following are some useful regulatory websites accorss the globe.
Clinical Research, Pharmacovigilance (PV) and Regulatory Website Listing.
| Sl. No | Regulatory Authority (RA) / Independent Authority (IA) | RA/IA | Regulatory Authority Links & Sub Links | Brief Explanation regarding the link | |
|---|---|---|---|---|---|
| Europe | |||||
| 1 | European Medicine Agency (EMA) | RA | http://www.ema.europa.eu/ema/ | This link includes patient safety, new medicines and public consultations (link sub tabs includes find medicine, human regulatory, veterinary regulatory, committee, news and events, partners and networks) | |
| 2 | European Medicine Agency (EMA) | RA | http://www.ema.europa.eu/ema/ index.jsp?curl=pages/about_us/ general/general_content_000217.jsp |
This links includes ommittees, working parties and other groups | |
| 3 | European Medicine Agency (EMA) | RA | http://www.ema.europa.eu/ema/ index.jsp?curl=pages/regulation/landing/ human_medicines_regulatory.jsp |
This links provides information for companies and individuals involved in developing and marketing medicines for human use in the European Union (EU). | |
| 4 | Medicines & Healthcare products Regulatory Agency (MHRA, UK) | RA (National Competent Authority) | https://www.gov.uk/government/ organisations/medicines-and- healthcare-products-regulatory-agency |
This link includes Drug and Device alert, Drug safety updates, Report a problem with a medicine or medical device, Blood regulation and safety, Marketing authorizations and licensing guidance, Patient information leaflets and summaries of product characteristics, Drug Analysis Prints (DAPs), Public assessment reports and Medical devices regulation and safety Contact MHRA and All MHRA services and information. | |
| 5 | Medicines & Healthcare products Regulatory Agency (MHRA, UK) | RA (National Competent Authority) | https://www.gov.uk/ drug-safety-update |
This link includes Drug safety updates | |
| 6 | Federal Agency for Medicines and Health Products (Belgium) | RA (National Competent Authority) | http://www.fagg-afmps.be/en/ | This link includes human medicine, veterinary medicines information for the public notification of adverse reactions or incidents. | |
| 7 | State instituute for drug control (Czech Republic) | RA (National Competent Authority) | http://www.sukl.eu/index.php | This link includes medicines, medical devices, pharmacies, healthcare facilities, pharmaceutical industries, distribution and functions of State institute for drug control | |
| 8 | National Agency for the Safety of Medicine and Health Products (France) | RA (National Competent Authority) | http://ansm.sante.fr/ | This link includes health products, report an adverse reactions, services, publications, records, activities and function of ANSM (National Agency for the Safety of Medicine and Health Products). | |
| 9 | Federal Institute for Drugs and Medical Devices (Federal Institute for Drugs and Medical Devices) | RA (National Competent Authority) | http://www.bfarm.de/EN/ Home/home_node.html |
This link includes about Bfarm agnecy, medicinal products, medical device, Federal opium agency, research and services. | |
| 10 | Italian Medicines Agency | RA (National Competent Authority) | http://www.agenziafarmaco .gov.it/en |
This link includes about AIFA, activities and director general. | |
| 11 | Spanish Agency for Medicines and Health Products | RA (National Competent Authority) | http://www.aemps.gob.es/ | This link includes Surveillance, clinical research, legislation and publications | |
| 12 | Medical Products Agency (MPA) | RA (National Competent Authority) | https://lakemedelsverket.se/ | This link includes health care, pharmacy and trade, public, Business, press | |
| 13 | Swiss Agency for Therapeutic products | RA (National Competent Authority) | https://www.swissmedic.ch/ index.html?lang=en |
This link includes news, medicinal product information, medical devices, authorizations, licensing, market surveillance and functions of agency | |
| North and South America | |||||
| 14 | The Brazilian Health Surveillance Agency (ANVISA-Brazil) | RA | http://portal.anvisa.gov. wps/portal/anvisa-ingles |
This link includes health protection, education and knowledge, news, post marketing surveillance and about agency. | |
| 15 | Health Canada (Canada) | RA | http://www.hc-sc.gc.ca/ index-eng.php |
This link includes about health Canada, consumer product safety, drugs and health products, environmental and work health, food nutrition and science and research. | |
| 16 | USA (U.S. Food and Drug Administration) | RA | http://www.fda.gov/ | This link includes about food, drug, medical devices, radiation-emitting products, vaccines, blood and biologics, animal and veterinary, cosmetics and tobacco products | |
| Asia, The Middle East and Ocean | |||||
| Vietnam | |||||
| 17 | Drug administration of Vietnam (Vietnam RA) | RA | http://www.dav.gov.vn/ Default.aspx |
English version is under construction | |
| Australia | |||||
| 18 | Therapeutic Goods Administration (TGA), Australia | RA | https://www.tga.gov.au/ | This link gives information on safety, useful information to health professionsal & consumers, pharmaceutical industry & regulatry authority in Australia. | |
| China | |||||
| 19 | China Food and Drug Administration (CFDA) | RA | http://eng.sfda.gov.cn/ WS03/CL0755/ |
This link provides information about CFDA, regulatory guide to medical devices, imported products, drug law, food & cosmetics in China. | |
| Egypt | |||||
| 20 | Egyptian Drug Authority (EDA | RA | http://www.eda.mohealth.gov.eg/ | This link provides information about Egyptian Drug Authority (EDA), legislation, safety & quality etc. | |
| Indonesia | |||||
| 21 | The National Agency of Drug & Food Control (NA-DFC) | RA | http://www.pom.go.id /index.php/home/en |
This link provides information about Indonesia regulatory authority (NA-DFC). | |
| Pakistan | |||||
| 22 | Drug Regulatory Authority of Pakistan (DRAP) | RA | http://www.dra.gov.pk/gop /index.php?q=aHR0cDov LzE5Mi4xNjguNzAuMTM2L2RyYXAv |
This link gives information about 1.Drug Regulatory Authority of Pakistan Act, 2012, 2. Drugs Act, 1976 3. SROs4. The Drugs (Labelling and Packing) Rules, 19865. The Drugs (Licensing, Registering & Advertising) Rules, 19766. The Drugs (Appellate Board) Rules, 19767. The Drugs (Research) Rules, 19788. The Drugs (Federal Inspectors, Federal Drug Laboratory & Federal Government Analysts) Rules, 19769. The Drugs (Imports & Exports) Rules, 197610. The Drugs (Specifications) Rules, 197811. The Northern Areas Drugs Rules, 199612. Pharmacy Act, 1967 | |
| Philippines | |||||
| 23 | Food And Drug Administration Philippines | RA | http://www.fda.gov.ph/ about-food-and-drug-administration |
This link provides general infrormation Philippines drug regulatory authority. | |
| 24 | Food And Drug Administration Philippines | RA | http://www.fda.gov.ph/consumers-corner/registered-drugs-2 | This link provides infrormation on drugs approved in Philippines. | |
| 25 | Food And Drug Administration Philippines | RA | http://www.fda.gov.ph/ | This link provides infrormation on registered vaccines and biological products in Philippines. | |
| Korea | |||||
| 26 | Korea Food and Drug Administration (KFDA) | RA | http://eng.kfda.go.kr/index.html | This link provides general infrormation Korea drug regulatory authority. | |
| Japan | |||||
| 27 | Pharmaceuticals & Medical devices Agency (PMDA) | RA | http://www.pmda.go.jp/english/ | This link provides the information pertaining to the Regulatory authority (Japan specific), information useful for healthcare professionals, academic information related to pharmaceuticals & pharmaceuticals business purpose. This link also gives information related to the postmarketing safety measures, releif services for adverse health effect, regulatory science & standard development, & international activities. | |
| Other Links - Useful Websites and Professional Organizations | |||||
| The International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) | http://www.ich.org | ||||
| The National Cancer Institute (NCI) and clinical trails | http://www.cancer.gov/clinicaltrials | ||||
| ClinicalTrials.gov - registry and results database of publicly and privately supported clinical studies of human participants conducted around the world. | http://www.clinicaltrials.gov/ | ||||
| Source for Clinical Research Information and Data | http://www.centerwatch.com/ | ||||
| Clinical Research and the HIPAA Privacy Rule | http://privacyruleandresearch.nih.gov/clin_research.asp | ||||
| E6 Good Clinical Practice Consolidated Guidance | http://www.fda.gov/ RegulatoryInformation/Guidances/default.htm |
||||
| Association of Clinical Research Professionals | www.acrpnet.org | ||||
| Regulatory Affairs Professional Society | www.raps.org | ||||
| American Medical Writer Association | www.amwa.org | ||||
| American Association of Pharmaceutical Scientists | www.aaps.org | ||||
| Society for Clinical Data Management | www.scdm.org | ||||
| Source of Information | Website link |
|---|---|
| The largest independent vendor in the business intelligence market | http://www.sas.com/ |
| SAS Press and SAS Documentation Example Code and Data | http://support.sas.com/ |
| Related to Clinical SAS | |
| Global, open, multidisciplinary, non-profit organization that has established standards to support the acquisition, exchange, submission and archive of clinical research data and metadata | http://www.cdisc.org/ |
| U.S. Food and Drug Administration (FDA) | http://www.fda.gov |
| ClinicalTrials.gov - registry and results database of publicly and privately supported clinical studies of human participants conducted around the world. | http://www.clinicaltrials.gov/ |
| EMEA | http://www.ema.europa.eu |
| Society for Clinical Data Management | http://scdm.org/ |
The mentorship supports our students in the career advancement. The QPDC provides real word learning experience and helps students in goal achievement. We mentor our students prior to training selection, during the training, and upon training completion.
Before the course registration, all candidates are mentored and advised in accordance to program's qualifications, available career opportunities, hiring trends, and pathways that are suitable to their education and experience in a given profession.
During the training students are assisted by the faculties in respect to additional project queries and other questions related to the program and real time experience.
Lastly, after the training students are receiving "post training support", which includes: "interview preparation and job search support", and "job assistance and placement support.
Join hands with Qtech and become leading company to provide Clinical Research, Clinical Data Management, Clinical SAS & Pharmacovigilance services to pharmaceutical and healthcare industry.
Qtech Specialize in developing and deliver Job Oriented Internship and Training Programs to professionals and fresh students to get familiar with client setting, tasks assigned and work culture of Title based jobs. Our programs best suit candidates having urge to make career pathways and looking to expand career opportunities as highly skilled professionals in Clinical Science and Healthcare Business Domains. The programs are delivered using various simulation methods to meet the job specific requirements. The focus is meeting client's needs, industry trends, current regulations, and positions in demand. All programs are supervised and conducted by industry professionals. Qtech University Alliance programs meets the compliance and follow the guidelines required.
Clinical Research is a rapidly expanding field, creating exciting job opportunities. Clinical Data Management (CDM) and Drug safety / Pharmacovigilance is the fastest growing and possibly the most profitable segment in Bio Services industry. The global clinical trial service market was worth an estimated $38.4 B in 2015, and is expected to grow up to $64 B by 2020. Over 70% of all clinical trial services will be outsourced by 2020, which is nearly 3 of every 4 clinical trials conducted.
QTECH SOLUTIONS INC, Doing Business As "Qtech-Sol Professional Development Center" (QPDC) is a Professional and Management Development Training Organization (NAICS 611430). We develop various Job Oriented Training Programs to individual students, looking to expand career opportunities as highly skilled professionals. E-verified with Immigration.
The Training's are provided to individuals and corporate through employers training programs and to those who have been recommended and approved by NJ Workforce. Our courses are customized and modified to meet the job market. Our Instructions is provided thru our custom-built Learning Management System as distance-learning (Online). The training provided has simulation methods and client settings required for student online learning.
Approved
Our Clinical Science Programs are Approved by New Jersey Department of Education and NJ Department of Labor and Workforce Development.
Program Delivery Models:
Current Programs
Unpaid Internship programs
Franchiser Licensee Support
We as Clinical Data Management Organization, provide product development services to the pharmaceutical, biotechnology, and medical device industries getting involved in approximately two-thirds of all Phase I - IV clinical trials, Our CDM professionals bring their scientific, regulatory and information management expertise to bear for the completion of timely, accurate, cost-effective trials and even controlling costs and reducing the research and development timelines.
Services Offered:
Qtech solutions is expertise in biostatistics and statistical programming in pre-clinical, phase I-IV clinical trials and post-marketing studies.
Our team of statistician have experience in designing and analyzing highly complex clinical trials. They are available to work with our clients in the study design stages, in interim analysis situations if needed and in the final statistical analysis and reporting stages of successfully completed studies. We provide comprehensive statistical services specifically designed to meet the needs of your study. Our experienced biostatisticians can design, perform quantitative analyses, and report on clinical trials in a broad range of therapeutic areas.
Bio-Statistical services:
Statistical Programming:
Our Cloud based narrative analytics product "Hiddime" (Hidden Dimensions), based on Semantics Technology is delivered along with its technical partners "Lead Semantics" and "Franz Inc". No programming or coding required, Connect and integrates all traditional (Oracle, Sql Server etc.) and non-traditional databases (LinkedIn, Facebook, Twitter etc.) into one platform. New generation SaaS based IDEA (Interactive Data Exploratory and Analytics) tool. Uses Semantic Computing solution allowing users to create semantically enriched data. Works in line with BI Data Warehouses, Data Lakes and the new Smart Big Data Lakes. Enhanced Data Discovery – Connected Graph enables Exploratory navigation by end business users. Includes Standard Visualizations Charts, Plots, Connected Graphs Role Based Access, Work Groups, Remote Concierge Data Analysis & Science. Meeting ROI and eliminate gaps. Get In-line reports online (anywhere and anytime) thru your mobile or on-site. Sync data and reports with time. Graphic visual analytics and dashboard for Financial, Banking, Sales, Marketing, Retail, Manufacturing, Staffing, Recruitment, Pharmaceutical , Hospitals, Healthcare and Insurance organizations.
Business Intelligence (BI) is a mature decades old enterprise practice. It is a set of systems working in tandem to deliver reports and dash-boards to upper management to help in communicating the state of the business, predominantly centered around performance indicators highlighting key areas of operations; resource utilization, sales and revenue realization and other delivery commitments the organization undertakes.
Qtech Solutions Inc, along with its technical collaboration with Lead Semantics and Franz Inc. believes significant new efficiencies especially supporting ease-of-use and delivering new types of analytics outcomes and insights can be delivered by a separate layer for data organization specific to serve visualization needs, and has recognized it as a business opportunity. Thus, hiddime lays special emphasis and has a built-in support for Data Organization for Visualizations and User Interactions.
Over the last decade, the data land scape in the enterprise has rapidly changed along with changing user and market expectations attached to the BI and Analytics off the data that is newly available. The unprecedented and exponential growth of sophisticated internet/web enabled consumer devices (smartphones, etc.) that are capable computers themselves, generating vast amounts of data and powerful computer and communication technologies along with potent software techniques such as graph processing and machine learning has enabled ever-complex processing work-loads generating deeper insights - defining characteristic of BIG DATA!
Hadoop as the defacto processing platform has dominated this new land scape, with recent addition of Spark for in-memory computation for advanced analytics among other platforms and frameworks.
Smart Data More recently, adding semantics to data during the ingest process (process of turning Big Data into Smart Data) has been proven to enhance manageability and governance of data as well as proven to reduce ETL work and frees up data scientists to maximize using their special skills to work on the advanced analytics that the organization wants delivered. Another major benefit of adding semantics to BIG DATA is that rich Knowledge Bases that exist in virtually every domain can be integrated and leveraged for deeper and more integrated analytics. Semantic integrated environments also drive up automation levels resulting in further efficiencies within the organization.
Hiddime is a new age BI and Analytics tool that has as its product focus the two areas:
Hiddime is an IDEA tool, Interactive Discovery, and Exploratory Analytics tool.
Hiddime differentiates itself from the usual BI tools with its focus on ease-of-use. Our emphasis on making the user interaction sessions seamless and simple has resulted in least learning curves for the business user. Typically, no more than few hours of training are required even for non-IT folks from various domains to operate and generate expert level analytics from data! Hiddime is domain and industry agnostic.
Higher levels of ease-of-use are made possible by two key ideas:
Business users and frontline managers who are not necessarily IT savvy, who know and understand their data and importantly can bring their gut feel based on their knowledge of the business context that allows them to discover organizational data that substantiates and supports decisions they take to advance corporate goals.
Unlike the typical BI tool Hiddime is not tied to RD and Multi-Dimensional Data warehouse, it is designed ground up to work with the newer data storage solutions from the BIGDATA world; NoSQL, Graph, Hybrid Store, Column Store and RDF Stores.
Hiddime in production uses a home-grown high-performance hybrid data storage with support for tables and edges for connected graphs. Soon, a new version of hiddime with support for RDF Triple Store as the storage backend is going to be released making hiddime first BI and Analytics product for Smart Data.
Visual Analysis using RDF Storage Data.
Hiddime Advantage
Qtech's Primary Consulting services include providing corporate training and supporting its clients with right candidate to meet their contractual and full-time human resource needs. We support various consultants towards Clinical Research, Drug Safety / Pharmacovigilance, Business Analysis, Reporting, Medical Writing and Safety Reviewers. Support towards Clinical Trial, Monitoring and Medical Safety, Healthcare Business and Project management services for pharmaceutical Research, Hospital, Medical Healthcare, Financial and Investment Banking firms.
Our PLACEMENT division offers Internship and support to client by providing resources to meet cost efficiency, time saving, and commitment towards hiring solutions to various companies in pharmaceutical, healthcare, and financial segments. Qtech is an equal opportunity employer.
Most professionals hired by Qtech hold bachelor or master's degree in Health Care Administration, Public Health, Medicine, Pharmacy, Registered Nurse (RN), Pharmaceutical Chemistry, Computer Science and Information Technology, Biostatistics, Engineering, Economics, Statistics, Pharmaceutics, Pharmacology, Toxicology, Pharmaceutical Business and Industrial Chemistry and Masters in Business Administration.
Our project managers are responsible for the overall conduct of a clinical study, ensuring quality is delivered from beginning to end. They provide leadership and oversight to our study teams and serve as a single point of contact for our sponsors. Qtech offers comprehensive services that supports all clinical trials from Phase II to Phase IV, beginning with Study Start-up, Feasibility through the completion of the Study Clinical Report. We provide solutions that can provide you with trial efficiencies, all driven with the goal to complete your study on time and on-budget.
Most professionals hired and working at Qtech hold Bachelor or Master degree in Medicine, PharmD, Nursing (RN), Health Care Administration, Public Health, Pharmaceutical Engineering, Pharmaceutics, Pharmacology, Toxicology, Industrial Chemistry, Computer Science and Information Technology, Bioinformatics, Statistics & Biostatistics, Business Administration (Marketing). Our Objective is to support various pharmaceutical, healthcare and research organization by providing project management and staffing resources to meet cost efficiency, times saved and commitment to full-fill.
Services Offered:
Our project managers are client focused and in charge of the clinical team for the duration of your clinical trial or drug development program. With a company-wide standard for quality and integrity, Qtech encourages team ownership of each clinical trial and is dedicated to its successful execution.
Our Clinical Research Project Management Services are:
Our project managers are responsible for the overall conduct of a Safety study, ensuring PV and Clinical Quality Assurance, Reporting and Medical Writing and Reporting, Evaluation, and Assessment. They provide leadership and oversight to our study teams and serve as a single point of contact for our sponsors. Qtech offers comprehensive services that supports various Pharmacovigilance Operations on time and on-budget.
Our experienced Drug Safety Physicians, Drug Safety and Pharmacovigilance Officers support monitoring, data collection and analysis, and reporting of medical safety information for compliance and meet regulations imposed.
Services Offered:
Qtech Professional Development Center (QPDC) is a Private Vocational School (PVS) approved by New Jersey Department of Education and Department of Labor and Workforce Development.
We are one of selected professional training providers which offer professional occupational education and job training opportunities that have been approved by the appropriate State agency and listed on New Jersey State Eligible Training Provider list (ETPL).QPDC satisfied specific eligibility criteria established by both the State Employment and Training Commission (SETC) and the local Workforce Investment Board (WIB) to be eligible to receive students paid for with public funds. Based on given State approvals, many QPDC's students who are eligible for training grants receive 100% funding to join and successfully complete our job oriented training programs.
You can find us on New Jerseys Eligible Training Provider List (ETPL) by going to the states website at http://www.njtrainingsystems.org/ and select "get started & search for training".
To view professional training programs offered by QPDC that are eligible for New Jersey state training grants 'Click Here'.
To find out about eligibility factors for state training grants, please contact us at qpdc@qtechelearncenter.com or visit nearest One Stop Career Center 'Click Here'.
No. Prior to starting our program, each trainee needs to be screened and interviewed. The education background is required. Qtech is for individuals who want to develop new set of skills, gain additional experience, or desire career transition.
The essence of our professional job oriented programs is gaining experience and working on real time scenario projects. We do not provide any curriculum based training, thus certain education background is required. Qtech provides training based on industry requirements and job qualifications. After completing our training you are not only certified, but also have experience you were missing and you are already qualified for entry/mid level positions.
The length of the training depends on the candidate's qualifications and previous experience. The training takes from 45 days to 90 days and depends on type and advance level of the training.
Minimum of 75% score is required to pass the final test and receive the Certificate of Completion. If you fail, you should contact us immediately at qpdc@qtechelearncenter.com and 2nd attempt will be provided within next 7 days.
Most of our trainees are full time students or employees. The relocation is not required for successfully program completion. You have 24/7 access to the material.
We recommend minimum 2 hours a day.
Yes. Qtech are approved. Please approach one of your closes one stop center.
Yes. Qtech is E-verified and an Equal Employment Opportunities (EEO) provider. We support our international students working with Qtech on CPT and OPT status.
Yes. However, we need first to evaluate your eligibility. There are two factors we consider: (1) preselection prior to the training start - interview is required; (2) training performance - final training performance evaluation is required.
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